Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Nitrobenzyl chloride → 3-(4-Nitrobenzyl)-5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Nitrobenzyl chloride | HCID 7482 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 5-(3,4-Dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one | HCID 15340822 | — |
| 반응물 | 1-(3,4-Dimethoxyphenyl)-2-bromobutan-1-one | HCID 19357910 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 3-(4-Nitrobenzyl)-5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one | HCID 9801942 | — |
반응 단계
A solution of 2.8 g of 5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one ("A") [obtainable by reacting 1-(3,4-dimethoxyphenyl)-2-bromobutan-1-one with methyl hydrazinethioformate] in 150 ml of acetone is boiled with 3 g of 4-nitrobenzyl chloride in the presence of 4 g of potassium carbonate for eight hours. The insoluble residue is filtered off and the solution is concentrated. The residue is worked up in the conventional manner to give 3-(4-nitrobenzyl)-5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06025354 |
| 출처 데이터셋 | uspto-grants-2000_02 |
| ORD ID | ord-a5cc4f3b83ea4d32b1e3a389b1a8a367 |
| 출처 메모 | uspto-grants-2000_02 |