Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dimethylformamide → 6-(2-Chloro-2-propenyloxy)-4-methyl-2-n-hexylamino-pyrimidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | 2,3-Dichloropropene | HCID 6565 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | HCID 178444746 | HCID 178444746 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 6-(2-Chloro-2-propenyloxy)-4-methyl-2-n-hexylamino-pyrimidine | HCID 20488795 | — |
반응 단계
42.0 g 6-Hydroxy-4-methyl-2-n-hexylamino-pyrimidin (0.2 Mol), 27.6 g K2CO3 (0.2 Mol), 24.4 g 2,3-dichloro-1-propene (0.22 Mol) and 150 ml dimethylformamide are charged in a sulphonation flask. The mixture is heated for about 3 hours at a bath temperature of 110°, then cooled to room temperature and thereafter poured in 500 ml water. This mixture is extracted with ether, the ether extract dried with Na2SO4 and concentrated with the aid of a flask rotary vacuum evaporator at a temperature of up to 60°. The impure title compound is obtained as a brown oil, which is purified chromatographically with ether/hexane 1:3 on silicagel to give a yellow oil that slowly crystallises. m.p. 36°-37°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04402730 |
| 출처 데이터셋 | uspto-grants-1983_09 |
| ORD ID | ord-1d372a172d074845be52f95c6041b800 |
| 출처 메모 | uspto-grants-1983_09 |