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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53867생성일: 2026년 10월 23일

Diethyl Ether → 1-[(4R,4aR,7S,7aR,12bS)-7,9-dihydroxy-3-methyl-1,2,4,4a,7,7a,10,13-octahydro-4,12-methanobenzofuro[3,2-e]isoquinolin-9-yl]ethanone

https://huagongshe.com/ko/reaction/53867

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Acetic AnhydrideHCID 7918—
반응물MorphineHCID 5288826—
용매Sodium BicarbonateHCID 516892—
생성물1-[(4R,4aR,7S,7aR,12bS)-7,9-dihydroxy-3-methyl-1,2,4,4a,7,7a,10,13-octahydro-4,12-methanobenzofuro[3,2-e]isoquinolin-9-yl]ethanoneHCID 2221195080%

반응 단계

To a stirred suspension of morphine (4 g, 14 mmol) in 10% aqueous sodium bicarbonate (377 ml) was added acetic anhydride (19 ml) over 8.5 minutes. 15 minutes after the addition, ice cold water (300 ml) was added and the solution was extracted with dichloromethane (200 ml). The organic extract was washed with brine, dried over Na2SO4, and the solvent removed in vacuo to leave a sticky white residue. Trituration with ether gave 3-acetylmorphine (3.68 g, 80%). The corresponding 3-pivalyl, 3-isobutyryl, 3-propionyl and other 3-acyl derivatives of morphine were also prepared.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05621087
출처 데이터셋uspto-grants-1997_04
ORD IDord-0aa465a90faf45259833d00a44a98cf2
출처 메모uspto-grants-1997_04