Cuprous chloride dimethyl carbonate

Dimethyl carbonate [616-38-6] and dimethyl oxalate [553-90-2] are both obtained from carbon monoxide, oxygen, and methanol at 363 K and 10 MPa (100 atm) or less. The choice of catalyst is critical cuprous chloride (66) gives the carbonate (eq. 20) a palladium chloride—copper chloride mixture (67,68) gives the oxalate, (eq. 21). Anhydrous conditions should be maintained by removing product water to minimize the formation of by-product carbon dioxide. 

In some instances a carbon-carbon bond can be formed with C-nucleophiles. For example, 3-carboxamido-6-methylpyridazine is produced from 3-iodo-6-methylpyridazine by treatment with potassium cyanide in aqueous ethanol and l,3-dimethyl-6-oxo-l,6-dihydro-pyridazine-4-carboxylic acid from 4-chloro-l,3-dimethylpyridazin-6-(lH)-one by reaction with a mixture of cuprous chloride and potassium cyanide. Chloro-substituted pyridazines react with Grignard reagents. For example, 3,4,6-trichloropyridazine reacts with f-butyl-magnesium chloride to give 4-t-butyl-3,5,6-trichloro-l,4-dihydropyridazine (120) and 4,5-di-t-butyl-3,6-dichloro-l,4-dihydropyridazine (121) and both are converted into 4-t-butyl-3,6-dichloropyridazine (122 Scheme 38). 

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)] ... 

The second step is reduction of cupric methoxychloride with carbon monoxide to form dimethyl carbonate. Cuprous chloride is simultaneously regenerated. This reaction is illustrated in Eq. (48) ... 

Another reaction of significance involving methanol is the direct synthesis of dimethyl carbonate (DMC) by carbonylation of methanol with CO which offers a potentially green chemical replacement for phosgene which is used for polymer production and other processes. The direct synthesis of dimethyl carbonate has been pursued over a variety of carbon supported cuprous chloride catalysts, but these catalysts deactivate due to loss of chloride and as such require reactivation by drying and contact with gaseous HCl. King et discovered that the chloride is not necessary to catal-... 

As was reported by Romano et aL, cuprous chloride is an effective catalyst for selective dimethyl carbonate synthesis. The reaction proceeds at 90—100 C at >20 bar of CO and can be either separated into an oxidation and a reduction step, or carried out in a one-pot redox system [71]. Dimethyl carbonate is a versatile reagent which can replace phosgene and dimethyl sulfate as carbonylating and methylating agents, respectively. 

Since sodium borohydride usually does not reduce the nitrile function it may be used for selective reductions of conjugated double bonds in oc,/l-un-saturated nitriles in fair to good yields [7069,1070]. In addition some special reagents were found effective for reducing carbon-carbon double bonds preferentially copper hydride prepared from cuprous bromide and sodium bis(2-methoxyethoxy)aluminum hydride [7766], magnesium in methanol [7767], zinc and zinc chloride in ethanol or isopropyl alcohol [7765], and triethylam-monium formate in dimethyl formamide [317]. Lithium aluminum hydride reduced 1-cyanocyclohexene at —15° to cyclohexanecarboxaldehyde and under normal conditions to aminomethylcyclohexane, both in 60% yields [777]. 

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