Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2,3,6-Trichlorobenzoic acid → (Aminocarbonyl)Methyl 2,3,6-Trichlorobenzoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2,3,6-Trichlorobenzoic acid | HCID 5759 | — |
| 반응물 | Chloroacetamide | HCID 6580 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 18-Crown-6 | HCID 28557 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (Aminocarbonyl)Methyl 2,3,6-Trichlorobenzoate | HCID 2417794 | — |
반응 단계
This compound was prepared in the manner of Example I, using 15.0 grams (0.066 mole) of 2,3,6-trichlorobenzoic acid, 4.4 grams (0.066 mole) of potassium hydroxide, 6.2 grams (0.066 mole) of 2-chloroacetamide, and 1.8 grams of 1,4,7,10,13,16-hexaoxacyclooctadecane in 300 ml of dry toluene and 200 ml of dimethylformamide. The crude product was purified by liquid chromatography, followed by recrystallization from ethyl acetate. The yield was 0.9 gram of (aminocarbonyl)methyl 2,3,6-trichlorobenzoate; mp 158°-160°. The ir and the nmr spectra were consistent with the proposed structure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04309566 |
| 출처 데이터셋 | uspto-grants-1982_01 |
| ORD ID | ord-f67ddac55063423aa6c6229eb1daa2d8 |
| 출처 메모 | uspto-grants-1982_01 |