Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → N-(alpha-cyanofurfuryl)-2,4-dimethylthiazole-5-carboxylic acid amide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Triethylamine hydrochloride | HCID 11130 | — |
| 반응물 | 2-Furanacetonitrile, alpha-amino- | HCID 11147706 | — |
| 반응물 | 2,4-Dimethylthiazole-5-carbonyl chloride | HCID 14653140 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-(alpha-cyanofurfuryl)-2,4-dimethylthiazole-5-carboxylic acid amide | HCID 14579913 | 90% |
반응 단계
In 120 ml of ethylacetate were dissolved 6.2 g of alpha-(2-furyl)-alpha-aminoacetonitrile and 6.0 g of triethylamine, and with stirring, the 2,4-dimethylthiazole5-carboxylic acid chloride was added dropwise to the solution, and the mixture was stirred at room temperature for 1 hour. Water (150 ml) was added, and the precipitated triethylamine hydrochloride was dissolved. The ethyl acetate layer was separated, washed with water, and dried over sodium sulfate. The dried ethyl acetate layer was distilled under reduced pressure to remove the solvent. The residue was recrystallized from isopropyl ether to give 11.65 g (yield 90.0%) of the desired N-(alpha-cyanofurfuryl)-2,4-dimethylthiazole-5-carboxylic acid amide.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05104886 |
| 출처 데이터셋 | uspto-grants-1992_04 |
| ORD ID | ord-eb2400d6d07f40b39555abfe687e9fa6 |
| 출처 메모 | uspto-grants-1992_04 |