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HRID 1375702作成日:2026年10月26日

Rofecoxib → (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol

https://huagongshe.com/reaction/1375702

反応式

関与物質

役割名称HCID仕込み量
反応物RofecoxibHCID 5090—
反応物Diisobutylaluminum hydrideHCID 14487—
反応物Sodium HydroxideHCID 14798—
溶媒DichloromethaneHCID 6344—
生成物(2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diolHCID 5743477398.7%

反応手順

To a solution of 110 g of 4-(4-methanesulfonyl-phenyl)-3-phenyl-5H-furan-2-one in 1.5 L of dichloromethane stirred at −78° C., 150 mL of DIBAL was added dropwise. The resulting mixture was warmed to room temperature and stirred overnight. The reaction mixture was then cooled to −78° C., and 1.2 L of 1 M aqueous NaOH was added dropwise. After the addition, the resulting mixture was warmed to room temperature and the organic phase was separated. The aqueous phase was extracted with dichloromethane. The organic phases were combined and dried over Na2SO4. 110 g of the titled compound was obtained after evaporation. 1H NMR (acetone-d6, 500 M Hz): δ 7.69 (d, 2H), 7.36 (d, 2H), 7.16–7.05 (m, 5H), 4.66 (d, 2H), 4.63 (d, 2H), 4.19 (t, 1H, OH), 4.17 (t, 1 H. OH), 3.04 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07169809B2
出典データセットuspto-grants-2007_01
ORD IDord-5edd1a315fdf4ebbb46c36c2676df4c7
出典メモuspto-grants-2007_01