戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 222187作成日:2026年10月26日

Acetic Acid → (R)-2-(((S)-3,3-Dimethyl-2,3-dihydro-1H-inden-1-yl)amino)-2-phenylethanol

https://huagongshe.com/reaction/222187

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物3,3-Dimethyl-1-indanoneHCID 304628—
反応物(R)-beta-aminophenethyl alcoholHCID 2724025—
反応物Sodium borohydrideHCID 4311764—
触媒p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒TolueneHCID 1140—
生成物(R)-2-(((S)-3,3-Dimethyl-2,3-dihydro-1H-inden-1-yl)amino)-2-phenylethanolHCID 6661825291.8%

反応条件

温度0 °C

反応手順

To a solution of 3,3-dimethylindan-1-one (925 mg, 5.77 mmol) and (R)-(−)-2-phenylglycinol (893 mg, 6.51 mmol) in toluene (10.0 mL) was added p-toluenesulfonic acid monohydrate (62.5 mg, 0.328 mmol). The reaction was heated to reflux under an atmosphere of nitrogen for 90 min. At this point, the mixture was cooled and diluted with toluene (10.0 mL). The mixture was washed with saturated aqueous sodium bicarbonate solution and water. The organic layer was concentrated in vacuo and the residue was dissolved in THF (10.0 mL) and cooled to 0° C. Acetic acid (1.13 mL, 19.9 mmol) was added, followed by sodium borohydride (251 mg, 6.64 mmol) and the reaction was allowed to warm to rt overnight. The mixture was partitioned between DCM and saturated aqueous sodium bicarbonate solution. The organic layer was concentrated and silica gel chromatography eluting with a gradient of 5 to 35% EtOAc in DCM afforded the title compound (1.49 g, 74%). LC/MS: Rt=1.92 min, ES+ 282 (AA standard).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207177B2
出典データセットuspto-grants-2012_06
ORD IDord-3d89567f7da2417cbe77edb6647d0cf3
出典メモuspto-grants-2012_06