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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4125Generated: October 23, 2026

Dimethyl Sulfide → 2-tert-Butyl-2-[(4-chlorophenoxy)methyl]oxirane

https://huagongshe.com/en/reaction/4125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantDimethyl SulfateHCID 6497—
Reactant2-Butanone, 1-(4-chlorophenoxy)-3,3-dimethyl-HCID 90518—
ReactantSodium MethoxideHCID 10942334—
SolventAcetonitrileHCID 6342—
Product2-tert-Butyl-2-[(4-chlorophenoxy)methyl]oxiraneHCID 1276362184%

Reaction Steps

A solution of 162 ml (2.2 moles) of dimethyl sulphide in 400 ml of absolute acetonitrile was added to a solution of 189 ml (2.0 moles) of dimethyl sulphate in 1,200 ml of absolute acetonitrile at room temperature. The reaction mixture was stirred overnight at room temperature. 118.8 g (2.2 moles) of sodium methylate were then added. The mixture was stirred for 30 minutes and a solution of 272 g (1.2 moles) of 1-(4-chlorophenoxy)-3,3-dimethyl-butan-2-one in 600 ml of absolute acetonitrile was then added dropwise in the course of 30 minutes. The reaction mixture was subsequently stirred overnight. It was then concentrated, the residue was partitioned between water and ethyl acetate, the organic phase was separated off, washed twice with water and once with saturated sodium chloride solution, dried over sodium sulphate and concentrated and the residue was distilled in vacuo. 242.4 g (84% of theory) of 2-(4-chlorophenoxymethyl)-2-tert.-butyl-oxirane of boiling point 115°-22° C./0.003 mm Hg column and of melting point 50°-52° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04723984
Source datasetuspto-grants-1988_02
ORD IDord-b9a65196066a45deb5cb3baa21f1de1c
Source noteuspto-grants-1988_02