참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | 3-Acetylbenzothiophene | HCID 14316 | — |
| 반응물 | 2-Propanol, sodium salt (1:1) | HCID 10920443 | — |
| 촉매 | Rhodium | HCID 23948 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | (1S)-1-(1-benzothiophen-3-yl)ethan-1-ol | HCID 25128401 | 99.5% |
반응 단계
To a solution of 4.45 g of 1-(1-benzothiene-3-yl)ethanone in 95 mL of isopropanol was added the asymmetric rhodium catalyst solution prepared as described above. Under reduced pressure (about 6600 Pa), an isopropanol solution of sodium isopropoxide (0.1 M, 10.0 mL) was added thereto. Further, the pressure was reduced to about 3700 Pa, followed by stirring at room temperature for 2 hours. To the reaction mixture was added acetic acid (2 mL) to stop the reaction, followed by concentrating under reduced pressure, and the residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain (1S)-1-(1-benzothiene-3-yl)ethanol (4.48 g, 94% ee) as a pale yellow oily substance. (HPLC analysis condition: CHIRALCEL OD-H column manufactured by (DAICEL CHEMICAL INDUSTRIES. Ltd., eluting solvent hexane/isopropanol=90/10, flow rate 1.0 mLmin−1, retention time: 8.1 min (S-isomer), 12.6 min (R-isomer)) EI: 178
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08153658B2 |
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| 출처 데이터셋 | uspto-grants-2012_04 |
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| ORD ID | ord-93327c6073574491a48036c309f6e91f |
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| 출처 메모 | uspto-grants-2012_04 |
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