Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium hydride → 4-(4-Methoxybenzylthio)nicotinic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-Methoxy-alpha-toluenethiol | HCID 80407 | — |
| 반응물 | 4-Chloronicotinic acid | HCID 818229 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(4-Methoxybenzylthio)nicotinic acid | HCID 14277652 | — |
반응 단계
A stirred and ice-cooled mixture of 788 mg (0.005 mole) 4-chloronicotinic acid [prepared by the process set forth in W. C. J. Ross, J. Chem. Soc.(C), 1816 (1966)]and 771 mg (0.005 mole) of 4-methoxybenzylmercaptan in 6 mL of dry N,N-dimethylformamide was treated with 480 mg (0.012 mole) of 60% sodium hydride dispersion. The reaction was stirred at room temperature for 4 hours during which a thick solid formed, which was taken up in 75 mL of ice water. After extraction with 25 mL of hexane, the aqueous layer was acidified with 2.5N hydrochloric acid to precipitate 4-(4-methoxybenzylthio)-nicotinic acid; yield 1.2 g (89% of theory), m.p. 230° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04767766 |
| 출처 데이터셋 | uspto-grants-1988_08 |
| ORD ID | ord-38fb0fdd2a2f47e8aaff7fe85e841c20 |
| 출처 메모 | uspto-grants-1988_08 |