Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133028생성일: 2026년 10월 25일
4-(Bromoacetyl)benzonitrile → 2-amino-5-(4-cyano-phenyl)-1H-pyrrole-3-carboxylic acid ethyl ester
https://huagongshe.com/reaction/133028
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-(Bromoacetyl)benzonitrile | HCID 98654 | — |
| 반응물 | Sodium ethoxide | HCID 2723922 | — |
| 반응물 | Ethyl 2-carbamimidoylacetate hydrochloride | HCID 15555354 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2-amino-5-(4-cyano-phenyl)-1H-pyrrole-3-carboxylic acid ethyl ester | HCID 69158918 | — |
반응 단계
A mixture of 42.53 g (0.255 mol) carbamimidoyl-acetic acid ethyl ester hydrochloride in 70 ml absolute ethanol is treated at 0 to 5° C. with 95.3 ml of a 21% sodium ethoxide solution in ethanol (0.255 mol) and stirred 5 min at 0 to 5° C. 4-Bromoacetyl-benzonitrile (28.6 g, 0.128 mol) is then added in portions over 20 min at 0 to 5° C. Stirring is continued at this temperature for 5 min then the ice bath is removed and the yellow suspension is stirred over night at RT. The solid is filtered off, washed with ethanol and ether and re-suspended in 450 ml actonitrile. The mixture is heated for 5 min under reflux, filtered while still hot and then cooled in an ice bath. The title compound is collected by succion and dried. Flash chromatography (dichtoromethane/ethyl acetate mixture) of the mother liquors gives an additional crop of the title compound as a yellow solid; m.p. 228-229° C.; MS-ES+: (M+H)+=254.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07390805B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-8e8d411034a346a3b031889df9058a94 |
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| 출처 메모 | uspto-grants-2008_06 |
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