참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Phenyl-2-(4-pyridinyl)ethanone | HCID 287104 | — |
| 반응물 | Ammonium Acetate | HCID 517165 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-Phenyl-2-(pyridin-4-yl)ethanamine | HCID 10465342 | 78.8% |
| 생성물 | Ammonia methanol | HCID 21705897 | 10% |
반응 단계
A mixture of (2) (1.98 g, 10.0 mmol), ammonium acetate (23.2 g, 300 mmol), and sodium cyanoborohydride (4.63 g, 69.9 mmol) in EPA (100 mL) was heated at 80° C. overnight. The mixture was evaporated under reduced pressure to remove IPA. The residue was diluted with water, and basified with NaOH (2M) to pH>7. The aqueous layer was extracted with dichloromethane (3×). The pooled organic layer was removed under vacuum. The residue was purified by chromatography on silica gel (100% ethyl acetate, then 10% saturated ammonia methanol in dichloromethane) to give 1-phenyl-2-(pyridin-4-yl)ethanamine (3) as a clear oil (0.780 g, 3.94 mmol, 39% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08809379B2 |
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| 출처 데이터셋 | uspto-grants-2014_08 |
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| ORD ID | ord-ab67822c53f44edd963ba7fa5ec2c3db |
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| 출처 메모 | uspto-grants-2014_08 |
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