참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 5-(2-bromoethyl)-2,3-dihydro-1H-indene | HCID 21224080 | — |
| 반응물 | 3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidine | HCID 22853758 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 3-(R)-(1-cyano-1,1-diphenylmethyl)-1-[2-(indan-5-yl)ethyl]piperidine | HCID 22853751 | — |
반응 단계
A mixture containing 3-(R)-(+)-(1-cyano-1,1,-diphenylmethyl)-piperidine (0.28 g), 5-(2-bromoethyl)indane (0.23 g--see Preparation 4), anhydrous potassium carbonate (0.3 g) and acetonitrile (10 ml) was heated under reflux for 5 hours. The mixture was partitioned between dichloromethane (30 ml) and 10% aqueous potassium carbonate (20 ml), the layers separated, and the aqueous layer extracted with dichloromethane (3×20 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give a gum which was purified by column chromatography on silica eluting with hexane containing dichloromethane (30% up to 70%) then dichloromethane containing methanol (0% up to 5%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from acetonitrile to give the title compound as colorless rhombs, yield 0.13 g, m.p. 88-91° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05932594 |
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| 출처 데이터셋 | uspto-grants-1999_08 |
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| ORD ID | ord-a344f509afcc4e73aee56e91e4dc4112 |
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| 출처 메모 | uspto-grants-1999_08 |
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