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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 447575생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/447575

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물3,3-Dimethyl-1-indanoneHCID 304628—
반응물(R)-beta-aminophenethyl alcoholHCID 2724025—
반응물Sodium borohydrideHCID 4311764—
촉매p-Toluenesulfonic acid monohydrateHCID 521998—
용매TolueneHCID 1140—
생성물(R)-2-(((S)-3,3-Dimethyl-2,3-dihydro-1H-inden-1-yl)amino)-2-phenylethanolHCID 6661825291.8%

반응 조건

온도0 °C

반응 단계

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 NaHCO3 solution and H2O. The organic layer was concentrated in vacuo and the residue was dissolved in THF (10.0 mL) and cooled to 0° C. AcOH (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 23° C. overnight. The mixture was partitioned between DCM and saturated aqueous NaHCO3 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481550B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-bc2d9f9578d0496e84365ec10dcdc6bc
출처 메모uspto-grants-2013_07