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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 863336생성일: 2026년 10월 24일

Hydrochloric Acid → (3R)-3-[(1R,7aR)-octahydro-4-bromomethylene-7a-methyl-1H-inden-1-yl]butanol

https://huagongshe.com/ko/reaction/863336

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DichloromethaneHCID 6344—
반응물Sodium SulfateHCID 24436—
반응물(3R)-3-[(1R,7aR)-octahydro-4-bromomethylene-7a-methyl-1H-inden-1-yl]butyronitrileHCID 70187237—
용매MethanolHCID 887—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물(3R)-3-[(1R,7aR)-octahydro-4-bromomethylene-7a-methyl-1H-inden-1-yl]butanolHCID 70187597—

반응 조건

온도-70 °C

반응 단계

A 84 mg amount of (3R)-3-[(1R,7aR)-octahydro-4-bromomethylene-7a-methyl-1H-inden-1-yl]butyronitrile was taken in a 25 ml eggplant-shaped flask, then 5 ml of dried dichloromethane was then added to dissolve the same. The solution was cooled by a -70° C. bath, then 660 μl of a 1.5 M [(CH3)2CHCH2 ]2AlH/toluene solution was added dropwise. The solution was stirred at the same temperature for 1 hour, then 0.5 ml of a saturated aqueous solution of sodium sulfate, 0.3 ml of methanol, 0.5 ml of 2 N hydrochloric acid, and 15 ml of ethyl acetate were added and the solution stirred for 30 minutes. The reaction solution was filtered by Celite, then was washed by a saturated solution of ammonium chloride and saturated saline, then was dried over anhydrous magnesium sulfate and the desiccant filtered out. The solvent was distilled off under reduced pressure to obtain (3R)-3-[(1R,7aR)-octahydro-4-bromomethylene-7a-methyl-1H-inden-1-yl]butanol in an amount of 85 mg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05719297
출처 데이터셋uspto-grants-1998_02
ORD IDord-bb88a666f16e42b68a3d81f342cf18c2
출처 메모uspto-grants-1998_02