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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 328333생성일: 2026년 10월 26일

Thiabendazole → 1-(2-Benzyloxyethoxycarbonyl)-2-(4-thiazolyl)-benzimidazole

https://huagongshe.com/reaction/328333

반응식

참여 물질

역할이름HCID투입량
반응물ThiabendazoleHCID 5430—
반응물2-Benzyloxyethyl chloroformateHCID 4563900—
반응물Pyridinium chlorideHCID 10176127—
용매PyridineHCID 1049—
생성물1-(2-Benzyloxyethoxycarbonyl)-2-(4-thiazolyl)-benzimidazoleHCID 21441722—

반응 단계

32.2 G. (150 mmoles) of 2-benzyloxyethylchloroformate is added dropwise with protection from moisture to a stirred suspension of 30.1 g. (150 mmoles) of 2(4-thiazolyl)-benzimidazole in 200 ml. of pyridine. The addition is complete in 30 minutes whereupon all of the starting material is dissolved and pyridine hydrochloride begins to precipitate. The reaction mixture is stirred at room temperature for 15 1/2 hours and filtered to remove pyridine hydrochloride. The solid material is washed with a small volume of pyridine and the combined filtrate and washing are evaporated to dryness in vacuo. The residual oil is dissolved in 300 ml. of methylene chloride and allowed to stand during which time a substantial amount of solid material precipitates. The solid is removed by filtration and the filtrate washed twice with 250 ml. of 0.25 N HCl containing ice followed by 200 ml. of saturated sodium bicarbonate solution containing 50 ml. of ice. The methylene chloride fraction is dried with magnesium sulfate, treated with charcoal, filtered and evaporated to dryness in vacuo affording 38.9 g. of a yellow-orange oil which begins to solidify on standing. The material is recrystallized from toluenecyclohexane affording 23.8 g. of 1-(2-benzyloxyethoxycarbonyl)-2-(4-thiazolyl)-benzimidazole, m.p. 93°-95° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04017503
출처 데이터셋uspto-grants-1977_04
ORD IDord-179c30dd96af4d33bcc359b2436b5e89
출처 메모uspto-grants-1977_04