Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616762생성일: 2026년 10월 25일
Carbamic acid, ethyl ester → 2-(3-ethoxycarbonyl-N-methyl-3-aza-propanamido)-5-chlorobenzophenone hydrochloride
https://huagongshe.com/reaction/616762
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbamic acid, ethyl ester | HCID 5641 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | N-(2-benzoyl-4-chlorophenyl)-2-bromo-N-methylacetamide | HCID 76099 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | 2-(3-ethoxycarbonyl-N-methyl-3-aza-propanamido)-5-chlorobenzophenone hydrochloride | HCID 70628768 | 158.8% |
반응 단계
7.3 g of 2-(N-methyl-bromoacetamido)-5-chlorobenzophenone are heated in 200 ml of anhydrous xylene with 2.2 g of triethylamine and 2 g of urethane (NH2COOC2H5) for 12 hours under reflux whilst stirring. The triethylamine hydrobromide which has precipitated is filtered off with suction after cooling, the filtrate is extracted by shaking with three times 250 ml of water and the organic phase is dried over potassium carbonate, filtered and evaporated in vacuo. The oily residue is dissolved in 400 ml of anhydrous diethyl ether and filtered and 6.5 g of 2-(3-ethoxycarbonyl-N-methyl-3-aza-propanamido)-5-chlorobenzophenone hydrochloride (79% of theory), with a melting point of 156°-158°, are obtained by passing dry hydrogen chloride gas into the ethereal solution.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04075409 |
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| 출처 데이터셋 | uspto-grants-1978_02 |
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| ORD ID | ord-6c8e637e7eac4613b994871ae2ec23ad |
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| 출처 메모 | uspto-grants-1978_02 |
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