돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 534703생성일: 2026년 10월 27일

Iodine → (alphaR)-alpha-[(1S)-2-(Dimethylamino)-1-methylethyl]-alpha-ethyl-3-methoxybenzenemethanol

https://huagongshe.com/reaction/534703

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물3-BromoanisoleHCID 16971—
반응물MagnesiumHCID 5462224—
반응물(2S)-1-(Dimethylamino)-2-methylpentan-3-oneHCID 11389445—
용매TetrahydrofuranHCID 8028—
생성물(alphaR)-alpha-[(1S)-2-(Dimethylamino)-1-methylethyl]-alpha-ethyl-3-methoxybenzenemethanolHCID 994297979.77%

반응 조건

온도71.5 °C

반응 단계

In a dry flask charged magnesium turning (41.0 gm 1.70 M) in tetrahydrofuran (200 ml). Under nitrogen atmosphere charged 3-Bromo anisole (20.0 gm; 0.106 M), iodine crystal (0.2 gm). Stirred and heated the reaction mass to 68-75° C. After initiation of the reaction the remaining quantity of 3-Bromo anisole (307 gm, 1.641 M) was added maintaining the reaction at reflux. Stirred and maintained the reaction mass at refluxed for 1 hrs, cooled to 25-30° C. Slowly added (2S)-1-(dimethylamino)-2-methylpentan-3-one (100.0 gm, 0.699 M) maintaining the temperature of the reaction at 25-30° C. The reaction mass was maintained for 12 hour at 25-30° C. and then quenched the reaction mass in ice cold D. M. water (1.0 Liter). Stirred and adjusted the pH of the reaction mass to 3-4 with acetic acid. Further adjusted the pH to 9-10 using ammonia solution. Stirred the reaction mass 30 minutes and extracted the reaction solution with diisopropyl ether. Combined diisopropyl ether was dried over anhydrous sodium sulphate and concentrated under reduced pressure below 40° C. to get the compound (2S,3R)-1-(dimethylamino)-3-(3-methoxyphenyl)-2-methylpentan-3-ol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853456B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-1330516c3e8149ae8345c9b8dcbe237f
출처 메모uspto-grants-2014_10