돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1607408생성일: 2026년 10월 26일

Phenylpropanolamine → (1S,2R)-2-amino-1-phenylpropan-1-ol

https://huagongshe.com/reaction/1607408

반응식

참여 물질

역할이름HCID투입량
반응물PhenylpropanolamineHCID 10297—
반응물2-(1-Naphthylmethyl)-6-phenylhexanoic acidHCID 13727091—
용매MethanolHCID 887—
생성물(1S,2R)-2-amino-1-phenylpropan-1-olHCID 2693466.1%

반응 조건

온도40 °C

반응 단계

A mixture of 5.0 g of (±)-2-(1-naphthylmethyl)-6-phenylhexanoic acid and 2.27 g of (-)-norephedrine was dissolved in 50 ml of methanol, and the mixture was concentrated under reduced pressure. The residue was dissolved in 60 ml of ethyl acetate with heating to 40° C. and the solution was allowed to stand overnight at room temperature. The precipitate was collected by filtration and recrystallized three times from ethyl acetate to obtain 1.5 g of the norephedrine salt (melting point 128°-131° C.). The resulting salt was dissolved in 30 ml of methanol, and 5 ml of a 1N-hydrochloric acid was added to the solution. The mixture was extracted with diethyl ether, and the ethereal layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to obtain 0.95 g of (+)-2-(1-naphtylmethyl)-6-phenylhexanoic acid as a colorless viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04863904
출처 데이터셋uspto-grants-1989_09
ORD IDord-d1e3147fb43d42f29be354744bda69ff
출처 메모uspto-grants-1989_09