Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Bromophenylhydrazine hydrochloride → ethyl 1-(3-bromophenyl)-5-tert-butyl-1H-pyrazole-3-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Bromophenylhydrazine hydrochloride | HCID 33757 | — |
| 반응물 | Ethyl 5,5-dimethyl-2,4-dioxohexanoate | HCID 83403 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | ethyl 1-(3-bromophenyl)-5-tert-butyl-1H-pyrazole-3-carboxylate | HCID 57428253 | 76.4% |
반응 단계
A solution of 3-bromophenylhydrazine hydrochloride (0.5 g, 2.2 mmol) and ethyl 5,5-dimethyl-2,4-dioxohexanoate (0.54 g, 2.68 mmol) in acetic acid (10 ml) was refluxed for 16 hours. The reaction was cooled to room temperature, and the solvent was removed under reduced pressure. The residue was partitioned between ethyl acetate and water. The organic layer was washed with water, saturated bicarbonate and brine, and dried over sodium sulfate, filtered and concentrated. The crude material was purified by column chromatography (4.8:0.2 hexanes/ethyl acetate) to give ethyl 1-(3-bromophenyl)-5-tert-butyl-1H-pyrazole-3-carboxylate (0.59 g, 74%) as a syrup.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07589116B2 |
| 출처 데이터셋 | uspto-grants-2009_09 |
| ORD ID | ord-610ff5fafba24af88484ecb8caab413b |
| 출처 메모 | uspto-grants-2009_09 |