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HRID 53867作成日:2026年10月24日

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/ja/reaction/53867

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Acetic AnhydrideHCID 7918—
反応物MorphineHCID 5288826—
溶媒Sodium BicarbonateHCID 516892—
生成物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]ethanoneHCID 2221195080%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05621087
出典データセットuspto-grants-1997_04
ORD IDord-0aa465a90faf45259833d00a44a98cf2
出典メモuspto-grants-1997_04