Dimethyl carbonate oxidation carbonylation

Aromatic polycarbonates are currently manufactured either by the interfacial polycondensation of the sodium salt of diphenols such as bisphenol A with phosgene (Reaction 1, Scheme 22) or by transesterification of diphenyl carbonate (DPC) with diphenols in the presence of homogeneous catalysts (Reaction 2, Scheme 22). DPC is made by the oxidative carbonylation of dimethyl carbonate. If DPC can be made from cyclic carbonates by transesterification with solid catalysts, then an environmentally friendlier route to polycarbonates using C02 (instead of COCl2/CO) can be established. Transesterifications are catalyzed by a variety of materials K2C03, KOH, Mg-containing smectites, and oxides supported on silica (250). Recently, Ma et al. (251) reported the transesterification of dimethyl oxalate with phenol catalyzed by Sn-TS-1 samples calcined at various temperatures. The activity was related to the weak Lewis acidity of Sn-TS-1 (251). [Pg.130]

The oxidative carbonylation of alcohols and phenols to carbonates can be catalyzed by palladium or copper species [154-213]. This reaction is of particular practical importance, since it can be developed into an industrial process for the phosgene-free synthesis of dimethyl carbonate (DMC) and diphenyl carbonate (DPC), which are important industrial intermediates for the production of polycarbonates. Moreover, DMC can be used as an eco-friendly methylation and carbonylation agent [214,215]. The industrial production of DMC by oxidative carbonylation of methanol has been achieved by Enichem [216] and Ube [217]. [Pg.259]

The oxidative carbonylation of methanol to dimethyl carbonate has found small industrial application (26-27). The reaction can be carried out in two steps following Equation 10 and 11 or also in one step. [Pg.10]

Biogenic processes, however, emit reduced forms of sulfur, including dimethyl sulfide and hydrogen sulfide, with lesser amounts of carbon disulfide (CS2), dimethyl disulfide (CH3SSCH3), carbonyl sulfide (COS), and methyl mercaptan (Cl I3SH). These reduced sulfur compounds are then oxidized in the atmosphere as described in detail in Chapter 8.E. [Pg.21]

Dimethyl Carbonate. An industrial process to manufacture dimethyl carbonate through the oxidative carbonylation of methanol catalyzed by cuprous chloride has been developed and commercialized by EniChem.197,198 The reaction occurs in two steps. Cupric methoxy chloride is formed in the first oxidation step [Eq. (7.21)], which is then reduced to yield dimethyl carbonate and regenerate cuprous chloride [Eq. (7.22)] ... [Pg.386]

In the case of experiments performed under the conditions of run 6, but in the presence of 1 ml of methanol, 1.6 equivalent of dimethyl carbonate was obtained according to GC analysis. No dimethyl carbonate was observed in the absence of hydrogen chloride. Therefore, in the early stage of the carbonylation of 3, Pd/C is partly oxidized to palladium chloride (eqn. 2). This compound reacts in turn with CO and MeOH to give, according to one of the routes described in Scheme 2, dimethyl carbonate and a zerovalent palladium complex (noted [Pd]). [Pg.266]

In the presence of trace amounts of water, the tetrameric p,2-oxo complex (182) in 1,2-dimethoxyethane is transformed into a p, -oxo tetrameric complex (183 equation 254), characterized by an X-ray structure.574 In contrast, (182) 572,575 is inactive towards the oxidation of phenols. The reaction of N,N,N, AT -tetramethyl-l,3-propanediamine (TMP) with CuCl, C02 and dioxygen results in the quantitative formation of the /z-carbonato complex (184 equation 255).s76 This compound acts as an initiator for the oxidative coupling of phenols by 02. 6 Such jz-carbonato complexes, also prepared from the reaction of Cu(BPI)CO with 02 [BPI = 1,3 bis(2-(4-methyl-pyridyl)imino)isoindoline],577 are presumably involved as reactive intermediates in the oxidative carbonylation of methanol to dimethyl carbonate (see below).578 Upon reaction with methanol, the tetrameric complex (182 L = Py X = Cl) produces the bis(/z-methoxo) complex (185 equation 256), which has been characterized by an X-ray structure,579 and is reactive for the oxidatiye cleavage of pyrocatechol to muconic acid derivatives.580,581... [Pg.389]

Oxidative carbonylation of MeOH with PdCl2 affords dimethyl carbonate (233) and dimethyl oxalate (232) [137,138], Selectivity of the mono- and dicarbonylation depends on CO pressure and reaction conditions. [Pg.446]

Oxidative Carbonylation of Methanol to Dimethyl Carbonate and Dimethyl Oxalate... [Pg.139]

Obviously only dimethyl carbonate is obtained in acceptable selectivities and space-time yields according to this method, although the analogous preparation of higher dialkyl carbonates and simple cyclic carbonates has also been described. Phenols do not give diaryl carbonates by CuCl-catalyzed oxidative carbonylation. [Pg.172]

Tomishige, K. Sakaihori, T. Sakai, S.-I. Fujimoto, K. Dimethyl carbonate synthesis by oxidative carbonylation on activated carbon supported CUCI2 catalysts catalytic properties and structural change. Appl. Catal. A. 1999,181, 95-102. [Pg.727]

King, S.T. Reaction mechanism of oxidative carbonylation of methanol to dimethyl carbonate in Cu-Y zelolite. J. Catal. 1996, 161, 530-538. [Pg.728]

Dimethyl carbonate (DMC) is a versatile compound that is an attractive alternative to phosgene [68, 69] and which could be synthesized in a eco-friendly process by catalytic oxidative carbonylation of methanol with oxygen (Enichem, Italy [70] and... [Pg.26]

Because of the toxicity of phosgene, research on nonphosgene routes to isocyanates and polycarbonates has intensified over the past decade. Eni-Chem of Italy has commercialized a process to manufacture dimethyl carbonate (DMC) by oxidative carbonylation of methanol. Dimethyl carbonate can be used as an intermediate for the production of polycarbonates. A description of the nonphosgenation chemistry for producing DMC and polycarbonates is included in Section II.A in this chapter. [Pg.233]

Oxidative carbonylation of methanol to dimethyl carbonate. Dimethyl carbonate (DMC) is made industrially by the phosgenation of methanol, but it can also be produced without the use of phosgene by the oxidative carbonylation of methanol. Enichem has commercialized a process for dimethyl carbonate based on oxidative carbonylation [25]. [Pg.252]

Cu-Catalyzed Oxidative Carbonylation of Methanol for the Synthesis of Dimethyl Carbonate... [Pg.72]

Palladium catalysts are widely used in liquid phase aerobic oxidations, and numerous examples have been employed for large-scale chemical production (Scheme 8.1). Several industrially important examples are the focus ofdedicated chapters in this book Wacker and Wacker-type oxidation of alkenes into aldehydes, ketones, and acetals (Scheme 8.1a Chapters 9 and 11), 1,4-diacetoxylation of 1,3-butadiene (Scheme 8.1b Chapter 10), and oxidative esterification of methacrolein to methyl methacrylate (Scheme 8.1c Chapter 13). In this introductory chapter, we survey a number of other Pd-catalyzed oxidation reactions that have industrial significance, including acetoxylation of ethylene to vinyl acetate (Scheme 8. Id), oxidative carbonylation of alcohols to dialkyl oxalates and carbonates (Scheme 8.1e), and oxidative coupling of dimethyl phthalate to 3,3, 4,4 -tetramethyl biphenylcarboxy-late (Scheme 8.1f). [Pg.115]

Oxidative carbonylation of alcohols in the presence of CO provides an economically viable route to dialkyl carbonates and/or oxalates (Eqs. (8.4) and (8.5)), both of which have important industrial applications. Dialkyl carbonates (e.g., dimethyl carbonate, propylene carbonate) are excellent solvents for a variety of organic substances [14]. Dialkyl oxalates have utility as solvents, C2 building blocks in fine chemicals synthesis, and intermediates in the manufacture of oxamide (as a fertilizer) [15]. Hydrogenation of dialkyl oxalates provides an alternative route to ethylene glycol that is independent of oil-derived resources [15,16]. [Pg.118]

A system has been described for the formation of dimethyl carbonate via the phosgene-free route of oxidative carbonylation of methanol [(Eq. (8)] catalyzed by PdCl2 in [BMIMKPFjj (110 C, total pressure 10 MPa, 1 h) [48]. Conversions were generally low (< 7%) and did not improve with increased reaction time, although the selectivity to dimethyl carbonate dropped. Dimethoxymethane was the major product but selectivities of dimethyl carbonate of up to 25% were possible with an O2/CO2 ratio of 29 71. Neither the pressure nor the temperature had dramatic effects upon the yield or selectivity, although the reaction was slower at lower temperatures. The reaction was repeated three times under the optimum conditions in a repetitive batch process. The rate remained constant, but there was a slight drop in selectivity. [Pg.704]

Reactions that require phosgene are dangerous, and dimethyl carbonate (DMC) 33 is the most promising phosgene substitute. Current industrial processes for DMC synthesis are oxidative carbonylation of methanol and transesterification of ethylene carbonate with methanol. Hence, the direct reaction of CO2 and methanol (Scheme 58) is regarded as an attractive, next-generation process, but the limitation... [Pg.155]

Indirect electrochemical oxidative carbonylation with a palladium catalyst converts alkynes, carbon monoxide and methanol to substituted dimethyl maleate esters (81). Indirect electrochemical oxidation of dienes can be accomplished with the palladium-hydroquinone system (82). Olefins, ketones and alkylaromatics have been oxidized electrochemically using a Ru(IV) oxidant (83, 84). Indirect electrooxidation of alkylbenzenes can be carried out with cobalt, iron, cerium or manganese ions as the mediator (85). Metalloporphyrins and metal salen complexes have been used as mediators for the oxidation of alkanes and alkenes by oxygen (86-90). Reduction of oxygen and the metalloporphyrin generates an oxoporphyrin that converts an alkene into an epoxide. [Pg.88]

Dimethyl carbonate (467) is produced under low pressure CO. Dimethyl carbonate is now produced commercially by Ube industries based on the oxidative carbonylation of MeOH in the gas phase using methyl nitrite (466) as an oxidant as shown below. Another promising reaction is the preparation of commercially important diphenyl carbonate (468) by the oxidative carbonylation of phenol. So far the technology developed in many industrial laboratories is far from commercialization [191]. [Pg.88]

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