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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4125생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfideHCID 1068—
반응물Dimethyl SulfateHCID 6497—
반응물2-Butanone, 1-(4-chlorophenoxy)-3,3-dimethyl-HCID 90518—
반응물Sodium MethoxideHCID 10942334—
용매AcetonitrileHCID 6342—
생성물2-tert-Butyl-2-[(4-chlorophenoxy)methyl]oxiraneHCID 1276362184%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723984
출처 데이터셋uspto-grants-1988_02
ORD IDord-b9a65196066a45deb5cb3baa21f1de1c
출처 메모uspto-grants-1988_02