Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 1-Methyl-beta-oxo-alpha-(p-methoxyphenylcarbamoyl)-2-pyrrolpropionitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-Isocyanato-4-methoxybenzene | HCID 79443 | — |
| 반응물 | 3-(1-Methyl-1H-pyrrol-2-yl)-3-oxopropanenitrile | HCID 2777170 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 1-Methyl-beta-oxo-alpha-(p-methoxyphenylcarbamoyl)-2-pyrrolpropionitrile | HCID 14555704 | — |
반응 단계
The suspension of 2.0 g of the 1-methyl-β-oxo-2-pyrrolpropionitrile in 50 ml of toluene and 1.6 g of triethylamine is treated with 2.1 g of p-methoxyphenylisocyanate. The mixture is warmed gently until all is dissolved and allowed to stand overnight at room temperature. It is evaporated, the residue is taken up in methanol and combined with 10 ml of 10% aqueous sodium hydroxide and 250 ml of water. The alkaline solution is filtered, acidified with 5 N hydrochloric acid and the precipitate formed collected. It is washed with water, dried, triturated with warm methanol-ethyl acetate, and recrystallized from ethyl acetate, to yield the 1-methyl-β-oxo-α-(p-methoxyphenylcarbamoyl)-2-pyrrolpropionitrile melting at 192°-193°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04256759 |
| 출처 데이터셋 | uspto-grants-1981_03 |
| ORD ID | ord-bd67a2403f5947ea99ebdfd823a2528c |
| 출처 메모 | uspto-grants-1981_03 |