참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diphenylacetonitrile | HCID 6837 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1-tosyl-3-(R)-(+)-tosyloxypiperidine | HCID 53865069 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | HCID 22853757 | HCID 22853757 | — |
반응 단계
Diphenylacetonitrile (13.5 g) was added to a stirred suspension of sodium hydride (3.2 g of a 60% suspension in mineral oil) in anhydrous toluene (250 ml) and the mixture was heated under reflux for 2 hours. On cooling to room temperature, 1-tosyl-3-(R)-(+)-tosyloxypiperidine (23 g) was added in portions and the mixture heated under reflux for 4 hours. The mixture was diluted with toluene (200 ml) and washed with 10% sodium hydroxide (2×100 ml) and brine (100 ml) then dried (MgSO4) and concentrated in vacuo to give an oil which was purified by column chromatography on silica eluting with toluene containing ethyl acetate (0% up to 10%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from ethanol to give the title compound, yield 16 g, m.p. 148°-150° C., [α]D25 -94.4° (c 1.0, CH2Cl2).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05422358 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-caa7ff901b584c6391dc33d4fdb072d6 |
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| 출처 메모 | uspto-grants-1995_06 |
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