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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22296생성일: 2026년 10월 24일

Sodium hydride → 3-(2,3-Dichlorophenylthiomethyl)-5-methyl-1,2,4-oxadiazole

https://huagongshe.com/ko/reaction/22296

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2,3-DichlorobenzenethiolHCID 140202—
반응물3-(Chloromethyl)-5-methyl-1,2,4-oxadiazoleHCID 302157—
용매TetrahydrofuranHCID 8028—
생성물3-(2,3-Dichlorophenylthiomethyl)-5-methyl-1,2,4-oxadiazoleHCID 1992865840.7%

반응 단계

7.0 g (39.1 mmol) of 2,3-dichloro-thiophenol are introduced into 50 ml of absolute tetrahydrofuran, the mixture is treated with 1.2 g (0.039 mmol) of 80% sodium hydride dispersion in portions and stirred for 2 hours at reflux temperature. The mixture is subsequently treated with 4.5 g (33.9 mmol) of 3-chloromethyl-5-methyl-1,2,4-oxadiazole at room temperature and stirred until the reaction is complete (approximately 10 to 15 hours). The sodium chloride which has precipitated is subsequently separated off and the entire batch is concentrated in vacuo. The crude product which remains can be chromatographed over a silica gel column (silica gel 60-Merck, particle size: 0.040 to 0.063 mm) using toluene as the eluent. 3.8 g (36.5% of theory) of 3-(2,3-dichlorophenylthiomethyl)-5-methyl-1,2,4-oxadiazole are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428047
출처 데이터셋uspto-grants-1995_06
ORD IDord-bfc60d7b03054bb0bd5938345113d8c0
출처 메모uspto-grants-1995_06