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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 745996생성일: 2026년 10월 26일

Carbon Dioxide → 2-(2,4-Dichlorobenzyloxy)-1-(1-imidazolyl)-3-(4-tert-butylphenylthio)propane

https://huagongshe.com/reaction/745996

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물2,4-Dichlorobenzyl chlorideHCID 7212—
반응물Sodium hydrideHCID 24758—
반응물1-(1-Imidazolyl)-3-(4-tert-butylphenylthio)-propan-2-olHCID 13688951—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-(2,4-Dichlorobenzyloxy)-1-(1-imidazolyl)-3-(4-tert-butylphenylthio)propaneHCID 13688952—

반응 조건

온도-20 °C

반응 단계

A dry 250-ml round bottom flask equipped with stir bar, addition funnel and N2 inlet was charged with dry dimethoxyethane (25 ml) and sodium hydride [60% (0.79 g, 0.0265 moles)]. The resulting slurry was cooled to -35° C. (with an external dry ice and acetone bath); then 1-(1-imidazolyl)-3-(4-tert-butylphenylthio)-propan-2-ol, 5.0 g (0.0172 moles), in 10 ml dry dimethoxyethane was added dropwise. After the addition was complete, the reaction mixture was allowed to warm to about -20° to -10° C. and was stirred at that temperature until no more H2 evolution was apparent. The reaction mixture was then cooled to -20° C. and 3.7 g (0.0189 mole) 2,4-dichlorobenzyl chloride were added very slowly. After the addition was complete, the reaction mixture was allowed to come to room temperature and was allowed to stir overnight. The reaction mixture was poured into water and ice and then extracted with ethyl acetate (twice). The ethyl acetate extracts were combined and washed with water until neutral. The ethyl acetate phase was dried, filtered, and then concentrated to give an oil which was chromatographed to give 2.0 g of the above-identified product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04602030
출처 데이터셋uspto-grants-1986_07
ORD IDord-7ee075dee3a04ef3a837192c90db801b
출처 메모uspto-grants-1986_07