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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 638312생성일: 2026년 10월 26일

4-Vinylbenzoic acid → 5-(4-vinylbenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid

https://huagongshe.com/reaction/638312

반응식

참여 물질

역할이름HCID투입량
반응물4-Vinylbenzoic acidHCID 14098—
반응물Methyl 2,3-dihydro-1H-pyrrolizine-1-carboxylateHCID 12795075—
용매O-XyleneHCID 7237—
생성물5-(4-vinylbenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acidHCID 1348706236%

반응 단계

A solution of methyl 1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylate (Formula B where Y is hydrogen) the synthesis of which is described in Preparations 1 and 2 hereinabove, (3.0 g, 18 mmol) and the acid chloride of 4-vinylbenzoic acid [J. Chem. Education, 55, 813 (1978)] (10.0 g, 60 mmol) in anhydrous xylene (100 ml) was heated at reflux temperature for 6 hours. The solvent was removed in vacuo and the residue was purified by column chromatography on Act II neutral alumina (Fluka, 200 g). The product was eluted with hexane-ethyl acetate (95:5) to give 5-(4-vinylbenzoyl)-1,2-dihydro-3H-pyrrolo[1,2,a]pyrrole-1-carboxylic acid, (36%) which had mp 99°-100° after crystallization from methanol. The purified product exhibited the following characteristics:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04560699
출처 데이터셋uspto-grants-1985_12
ORD IDord-f27f10d9392e45628b59d516299f3422
출처 메모uspto-grants-1985_12