Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 4-Phenyl-2-pyridinecarbonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Phenylpyridine-1-oxide | HCID 70803 | — |
| 반응물 | Trimethylsilyl cyanide | HCID 82115 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 4-Phenyl-2-pyridinecarbonitrile | HCID 87758 | — |
반응 단계
A solution of 1.90 g (11.1 mmol) of 4-phenylpyridine-N-oxide (available from Aldrich Chemical Co.), 4.8 ml (35 mmol) of sieve-dried triethylamine and 4.7 ml (35 mmol) trimethylsilylcyanide in 10 ml of sieve-dried acetonitrile was heated to 100° for 24 hours. The reaction mixture was cooled, quenched with 1 ml of H2O then added to 50 ml of H2O and extracted with three-25 ml portions of ethyl acetate. The organic extracts were combined, dried (MgSO4), concentrated in vacuo and purified by flash chromatography (silica gel, 1:4 EtOAc/petroleum ether) to give 2-cyano-4-phenylpyridine as a white solid. Recrystallization (EtOAc/petroleum ether) of the solid afforded 1.65 g (83%) of title nitrile as white crystals, m.p. 97°-98°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04555520 |
| 출처 데이터셋 | uspto-grants-1985_11 |
| ORD ID | ord-dce9f8a8f92d4bb09de767a3405114d7 |
| 출처 메모 | uspto-grants-1985_11 |