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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11209생성일: 2026년 10월 23일

Diethyl Ether → (2R,3R)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol

https://huagongshe.com/ko/reaction/11209

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Sodium HydroxideHCID 14798—
반응물Bupropion Morpholinol (2R,3R)-IsomerHCID 9943907—
용매WaterHCID 962—
생성물(2R,3R)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinolHCID 9943908—

반응 단계

(+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride may be converted back to its free base by the following process. A 3.0 g sample of (+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride was dissolved in water (100 mL) and diethyl ether was added (200 mL). The mixture was chilled in an ice bath and the pH was adjusted to >10 with 1.0N aqueous sodium hydroxide. After stirring for 30 min., the phases were separated and the aqueous phase was extracted with diethyl ether. The combined diethyl ether extracts were dried (Na2SO4) and concentrated in vacuo to give 2.6 g of (+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol as a white solid. This was used without further purification for the chiral chromatography described below.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098206B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-ccf1d5796b1247748d63c86e697ede67
출처 메모uspto-grants-2006_08