Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 2-[(E)-4-chloro-2-butenyloxy]-5-nitrobenzaldehyde
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 5-Nitrosalicylaldehyde | HCID 66808 | — |
| 반응물 | 1,4-Dichloro-2-butene, (2E)- | HCID 642197 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-[(E)-4-chloro-2-butenyloxy]-5-nitrobenzaldehyde | HCID 14050496 | 43.3% |
반응 단계
A solution of 8 g of 5-nitrosalicylaldehyde, 30.8 g of trans-1,4-dichloro-2-butene and 13.2 g of potassium carbonate in 35 ml of dimethylformamide was stirred at room temperature for 19 hours, and further stirred at 80°-87° C. (outside temperature) for 2 hours. The mixture was allowed to cool, poured into 80 ml of water, and extracted with chloroform. The extract (organic layer separated) was concentrated under reduced pressure. The residue was subjected to column chromatography on silica gel. The product was eluted with benzene to give 5.3 g of 2-[(E)-4-chloro-2-butenyloxy]-5-nitrobenzaldehyde. (mp. 65°-66° C.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04727082 |
| 출처 데이터셋 | uspto-grants-1988_02 |
| ORD ID | ord-42e9e6685d48461cbe538debba22bce7 |
| 출처 메모 | uspto-grants-1988_02 |