Chemistry:Chloroalkyl ether

From HandWiki
Chemical structure of chloromethyl methyl ether (MOM-Cl)

Chloroalkyl ethers are a class of organic compounds with the general structure R-O-(CH2)n-Cl, characterized as an ether connected to a chloromethyl group via an alkane chain.

Chloromethyl methyl ether (CMME) is an ether with the formula CH
3
OCH
2
Cl
. It is used as an alkylating agent and industrial solvent to manufacture dodecylbenzyl chloride, water repellents, ion-exchange resins, polymers, and as a chloromethylation reagent. In organic synthesis the compound is used for the introduction of the methoxymethyl (MOM) protecting group.

Closely related compounds of industrial importance are bis(chloromethyl) ether (BCME) (closely related to chemical weapon sulfur mustard)[1] and benzyl chloromethyl ether (BOMCl).

Chloromethyl ether R Molar mass CAS number Boiling point °C
Benzyl chloromethyl ether Benzyl benzyl chloromethyl ether 156.61 3587-60-8 102 °C @ 14 mmHg (1.9 kPa)
Chloromethyl methyl ether Methyl methyl chloromethyl ether 80.51 107-30-2 55-57
Bis(chloromethyl) ether Bis(chloromethyl) ether.svg 114.96 542-88-1 106
tert-Butyl chloromethyl ether Butyl T-Butoxymethyl chloride.svg 124.5
2-Methoxyethoxymethyl chloride Methoxyethoxymethyl chloride.svg 124.57 3970-21-6 50-52 °C @ 13 mmHg (1.7 kPa)
Dichloromethyl methyl ether Dichloromethyl methyl ether.svg 114.96 4885-02-3 82 - 85.5 °C
Representative chloroalkyl ethers[2]

Methoxymethyl ethers (MOMs) and methoxyethyl ethers (MEMs) are common protecting groups in organic synthesis.

Safety

Chloroalkyl ethers are strong alkylating agents with attendant dangers. These compounds are human carcinogen.[3]

References