戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1603276作成日:2026年10月27日

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

https://huagongshe.com/reaction/1603276

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DichloromethaneHCID 6344—
反応物Sodium SulfateHCID 24436—
反応物(3R)-3-[(1R,7aR)-octahydro-4-bromomethylene-7a-methyl-1H-inden-1-yl]butyronitrileHCID 70187237—
溶媒MethanolHCID 887—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物(3R)-3-[(1R,7aR)-octahydro-4-bromomethylene-7a-methyl-1H-inden-1-yl]butanolHCID 70187597—

反応条件

温度-70 °C

反応手順

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 1.5M [(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 2N 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05986112
出典データセットuspto-grants-1999_11
ORD IDord-ff5cb8dffb274ee1baaa3361b6c2bd3a
出典メモuspto-grants-1999_11