Dichlorocarbene

Carbon dichlorideCarbonous chlorideDichloro-λ2-methaneDichlorocarbene is the reactive intermediate with chemical formula CCl2. Although this material has not been isolated, it is a common intermediate in organic chemistry, being generated from chloroform. This bent diamagnetic molecule rapidly inserts into other bonds. Dichlorocarbene is the reactive intermediate with chemical formula CCl2. Although this material has not been isolated, it is a common intermediate in organic chemistry, being generated from chloroform. This bent diamagnetic molecule rapidly inserts into other bonds. Dichlorocarbene is most commonly generated by reaction of chloroform and a base such as potassium t-butoxide or aqueous sodium hydroxide. A phase transfer catalyst, for instance benzyltriethylammonium bromide, facilitates the migration of the hydroxide in the organic phase. Another precursor to dichlorocarbene is ethyl trichloracetate. Upon treatment with sodium methoxide it releases CCl2. Phenyl(trichloromethyl)mercury decomposes thermally to release CCl2. Dichlorodiazirine, which is stable in the dark, decomposes into dichlorocarbene and nitrogen via photolysis. Dichlorocarbene can also be obtained by dechlorination of carbon tetrachloride with magnesium with ultrasound chemistry. This method is tolerant to esters and carbonyl compounds because it does not involve strong base. Dichlorocarbene reacts with alkenes in a formal cycloaddition to form geminal dichlorocyclopropanes. These can be reduced to cyclopropanes or hydrolysed to give cyclopropanones by a geminal halide hydrolysis. Dichlorocyclopropanes may also be converted to allenes in the Skattebøl rearrangement. In the Reimer–Tiemann reaction dichlorocarbene reacts with phenols to give the ortho-formylated product. e.g. phenol to salicylaldehyde. Dichlorocarbene is an intermediate in the carbylamine reaction. In this conversion, a dichloromethane solution of a primary amine is treated with chloroform and aqueous sodium hydroxide in the presence of catalytic amount of the phase transfer catalyst. Illustrative is the synthesis of tert-butyl isocyanide: