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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 905063생성일: 2026년 10월 24일

Imidazole → Trans-1-{6-[alpha-(4-chlorophenyl)-2,4-dichlorobenzyloxy]tetrahydropyran-2-ylmethyl}imidazole

https://huagongshe.com/ko/reaction/905063

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물Sodium IodideHCID 5238—
반응물Sodium hydrideHCID 24758—
반응물Trans-6-[alpha-(4-chlorophenyl)-2,4-dichlorobenzyloxy]-2-tosyloxymethyltetrahydropyranHCID 53867744—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Trans-1-{6-[alpha-(4-chlorophenyl)-2,4-dichlorobenzyloxy]tetrahydropyran-2-ylmethyl}imidazoleHCID 1307392275.3%

반응 조건

온도80 °C

반응 단계

114 mg of 55% sodium hydride were added to a solution of 323 mg of imidazole in 10 ml of dimethylformamide, and, after the mixture had been stirred at 80° C. for 30 minutes, it was cooled to room temperature. There were then added 2.20 g of trans-6-[α-(4-chlorophenyl)-2,4-dichlorobenzyloxy]-2-tosyloxymethyltetrahydropyran, dissolved in 15 ml of dimethylformamide, and then 594 mg of sodium iodide were added to the mixture. The resulting mixture stirred under a stream of nitrogen at 90°-95° C. for 4 hours, after which it was cooled, diluted with water and extracted with diethyl ether. The ethereal extract was washed with water and dried over sodium sulphate, after which it was concentrated by evaporation under reduced pressure and the residue was purified by column chromatography through silica gel eluted with a 8:1:0.1 by volume mixture of ethyl acetate, benzene and triethylamine, to give 1.346 g of the title compound as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04421758
출처 데이터셋uspto-grants-1983_12
ORD IDord-480fb030c2094e639f142434abd29276
출처 메모uspto-grants-1983_12