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HRID 1291650作成日:2026年10月25日

tert-Butanol → 5-hydroxymethyl-5-hydroxy-1-(4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine

https://huagongshe.com/reaction/1291650

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物Trimethylamine oxide dihydrateHCID 198430—
反応物HCID 19608041HCID 19608041—
反応物Sodium BisulfiteHCID 23665763—
触媒Osmium TetroxideHCID 30318—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物5-hydroxymethyl-5-hydroxy-1-(4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepineHCID 1960796584.4%

反応手順

To 5-methylidene-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.60 g) are added successively t-butyl alcohol (6.0 ml), water (1.2 ml), pyridine (0.3 ml), osmium tetroxide (1.2 mg) and trimethylamine N-oxide dihydrate (0.22 g), and the mixture is refluxed with stirring for 2.5 hours. After cooling, to the reaction solution is added 20% aqueous sodium hydrogen-sulfite solution (10 ml), and the mixture is stirred at room temperature for 1.5 hour. The reaction solution is extracted with a mixture of ethyl acetate/tetrahydrofuran (1:1). The extract is washed successively with diluted hydrochloric acid and saturated saline solution, and dried over magnesium sulfate. The solvent is distilled off and the resulting residue is recrystallized from ethyl acetate/n-hexane to give 5-hydroxymethyl-5-hydroxy-1-(4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.55 g) as white powder, m.p. 136°-140° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05753677
出典データセットuspto-grants-1998_05
ORD IDord-9bbd47fa7fd346d6ab8600cc76f0198e
出典メモuspto-grants-1998_05