Dichlorocarbene

Dichlorocarbene is most commonly generated by reaction of chloroform and a base such as potassium tert-butoxide or aqueous sodium hydroxide. A phase transfer catalyst, for instance benzyltriethylammonium bromide, facilitates the migration of the hydroxide in the organic phase. :HCCl3 + NaOH → CCl2 + NaCl + H2O Other reagents and routes Another precursor to dichlorocarbene is ethyl trichloroacetate. Upon treatment with sodium methoxide it releases CCl2. Phenyl(trichloromethyl)mercury decomposes thermally to release CCl2. :PhHgCCl3 → CCl2 + PhHgCl Dichlorodiazirine, which is stable in the dark, decomposes into dichlorocarbene and nitrogen via photolysis. (b) hydroxylamine (c) mesyl chloride (d) sodium hypochlorite (e) nitronium tetrafluoroborate (f) caesium and tetrabutylammonium chlorides in an ionic liquid 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. ==Reactions==

With alkenes Dichlorocarbene reacts with alkenes in a formal [1+2]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. : Dichlorocarbene reacts with tetrachloroethylene to give hexachlorocyclopropane. A similar reaction occurs with trichloroethylene, yielding pentachlorocyclopropane. With phenols In the Reimer–Tiemann reaction dichlorocarbene reacts with phenols to give the ortho-formylated product. e.g. phenol to salicylaldehyde. : With amines 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: :Me3CNH2 + CHCl3 + 3 NaOH → Me3CNC + 3 NaCl + 3 H2O ==History==

In 1835, the French chemist Auguste Laurent recognised chloroform as • (then written as •) in his paper on analysing some organohalides. Laurent also predicted a compound seemingly consisting of 2 parts dichlorocarbene which he named Chlorétherose (possibly Tetrachloroethylene, which was not produced until 1839). Dichlorocarbene as a reactive intermediate was first proposed by Anton Geuther in 1862 who viewed chloroform as CCl2.HCl Its generation was reinvestigated by Jack Hine in 1950. The preparation of dichlorocarbene from chloroform and its utility in synthesis was reported by William von Eggers Doering in 1954. ==Related reactions==

The Doering–LaFlamme allene synthesis entails the conversion of alkenes to allenes (a chain extension) with magnesium or sodium metal through initial reaction of the alkene with dichlorocarbene. The same sequence is incorporated in the Skattebøl rearrangement to cyclopentadienes. Closely related is the more reactive dibromocarbene CBr2. ==Chlorocarbene==

The related chlorocarbene (ClHC) can be generated from methyllithium and dichloromethane. It has been used in the synthesis of spiropentadiene. ==See also==