Dichlorocarbene is the reactive intermediate with chemical formula CCl2. Although this chemical species 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.
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| Names | |||
|---|---|---|---|
| Preferred IUPAC name
Dichloromethylidene | |||
| Other names
Carbon(II) chloride
Carbon dichloride | |||
| Identifiers | |||
3D model (JSmol) |
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| 1616279 | |||
| ChEBI | |||
| ChemSpider | |||
| 200357 | |||
| MeSH | Dichlorocarbene | ||
PubChem CID |
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| UNII | |||
CompTox Dashboard (EPA) |
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| Properties | |||
| CCl2 | |||
| Molar mass | 82.91 g·mol−1 | ||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
Main hazards |
Highly reactive | ||
| Related compounds | |||
Related compounds |
C2Cl4 | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Dichlorocarbene is most commonly generated by reaction of chloroform and a base such as potassium tert-butoxide or aqueous sodium hydroxide.[1]Aphase transfer catalyst, for instance benzyltriethylammonium bromide, facilitates the migration of the hydroxide in the organic phase.
Another precursor to dichlorocarbene is ethyl trichloroacetate. Upon treatment with sodium methoxide it releases CCl2.[2]
Phenyl(trichloromethyl)mercury decomposes thermally to release CCl2.[3]
Dichlorodiazirine, which is stable in the dark, decomposes into dichlorocarbene and nitrogen via photolysis.[4]
Dichlorocarbene can also be obtained by dechlorinationofcarbon tetrachloride with magnesium with ultrasound chemistry.[5] This method is tolerant to esters and carbonyl compounds because it does not involve strong base.
Dichlorocarbene reacts with alkenes in a formal [1+2]cycloaddition to form geminal dichlorocyclopropanes. These can be reducedtocyclopropanes 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.[6] 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:[7]
In 1835, the French chemist Auguste Laurent recognised chloroform as CCl2•HCl (then written as C8Cl8•H4Cl4)[a] in his paper on analysing some organohalides. Laurent also predicted a compound seemingly consisting of 2 parts dichlorocarbene called Chlorétherose, Tetrachloroethylene, which was not known to exist at the time.[8]
Dichlorocarbene as a reactive intermediate was first proposed by Anton Geuther in 1862 who viewed chloroform as CCl2.HCl[9] Its generation was reinvestigated by Hine in 1950.[10] The preparation of dichlorocarbene from chloroform and its utility in synthesis was reported by William von Eggers Doering in 1954.[11]
The Doering–LaFlamme allene synthesis entails the conversion of alkenes to allenes (a chain extension) with magnesiumorsodium 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.
The related chlorocarbene (ClHC) can be generated from methyllithium and dichloromethane. It has been used in the synthesis of spiropentadiene.
