Dimethylcarbamoyl chloride is a reagent for transferring a dimethylcarbamoyl group to alcoholic or phenolic hydroxyl groups forming dimethyl carbamates, usually having pharmacological or pesticidal activities. Because of its high toxicity and its carcinogenicproperties shown in animal experiments and presumably also in humans, dimethylcarbamoyl chloride can only be used under stringent safety precautions.
The production of dimethylcarbamoyl chloride from phosgene and dimethylamine was reported as early as 1879. DMCC can be produced in high yields at 275 °C by reacting phosgene with gaseous dimethylamine in a flow reactor. To suppress the formation of ureas, excess phosgene is used. The reaction can also be carried out at the laboratory scale with diphosgene or triphosgene and an aqueous dimethylamine solution in the two-phase system of benzene–xylene and water in a stirred reactor with sodium hydroxide as an acid scavenger. However, considerably lower yields are achieved due to the hydrolysis sensitivity of DMCC. Dimethylcarbamoyl chloride is also formed when reacting phosgene with trimethylamine. A more recent process is based on chlorodimethylamine, which is converted practically quantitatively to dimethylcarbamoyl chloride on a palladium catalystunder pressure with carbon monoxide at room temperature. DMCC can also be formed in small amounts from dimethylformamide in the Vilsmeier–Haack reaction or when DMF is used as a catalyst in the reaction of carboxylic acids with thionyl chloride to the corresponding acyl chloride. The tendency towards DMCC formation depends on the chlorination reagent and is higher in the presence of a base. However, dicarbamoyl chloride hydrolyses very quickly to dimethylamine, hydrochloric acid and carbon dioxide so that less than 3 ppm of dicarbamoyl chloride is found in the Vilsmeier product after aqueous workup.
Properties
Dimethylcarbamoyl chloride is a clear, colorless, corrosive and flammable liquid with a pungent odor and a tear-penetrating effect, which decomposes rapidly in water. Because of its unpleasant, toxic, mutagenic and carcinogenic properties, it has to be used under extreme precautions. DMCC behaves like an acyl chloride whose chlorine atom can be exchanged for other nucleophiles. Therefore, it reacts with alcohols, phenols and oximes to the corresponding N,N-dimethylcarbamates, with thiols to thiolourethanes, with amines and hydroxylamines to substituted ureas, and with imidazoles and triazoles to carbamoylazoles. DMCC is less reactive and less selective to substrates with multiple nucleophilic centers than conventional acyl chlorides. Unsaturated conjugated aldehydes such as crotonaldehyde react with DMCC forming dienyl carbamates, which can be used as dienes in Diels–Alder reactions. Alkali metal carboxylates react with DMCC forming the corresponding dimethylamides. DMCC reacts with anhydrous sodium carbonate or with excess dimethylamine to form tetramethylurea. The reaction of DMCC with DMF forms tetramethylformamidinium chloride, which is a major intermediate in the preparation of trismethane, a reagent for the introduction of enamine functions in conjunction with activated methylene groups and the preparation of amidines. DMCC is a starting material for the insecticide class of the dimethyl carbamates which act as inhibitors of acetylcholinesterase, including dimetilane, and the related compounds isolane, pirimicarb and triazamate. The quaternary ammonium compoundsneostigmine finds pharmaceutical applications as acetylcholinesterase inhibitors. It is obtained from 3-phenol and DMCC and subsequent quaternization with methyl bromide or dimethyl sulfate and pyridostigmine, which is obtainable from 3-hydroxypyridine and DMCC and subsequent reaction with methyl bromide. DMCC is also used in the synthesis of the benzodiazepinecamazepam.
