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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258031생성일: 2026년 10월 26일

3',4'-Dimethoxycinnamic acid → 3,4-Dimethoxycinnamoylchloride

https://huagongshe.com/reaction/258031

반응식

참여 물질

역할이름HCID투입량
반응물3',4'-Dimethoxycinnamic acidHCID 16848—
반응물Oxalyl chlorideHCID 65578—
촉매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물3,4-DimethoxycinnamoylchlorideHCID 53399206—

반응 단계

To a mixture of 3,4-dimethoxycinnamic acid (540 mg), DMF (2 drops) and tetrahydrofuran (10 ml) was added oxalyl chloride (0.27 ml) dropwise. The mixture was stirred at room temperature for 40 minutes, at the end of which time the solvent was distilled off to give 3,4-dimethoxycinnamoyl chloride. The chloride was dissolved in dichloromethane (10 ml) followed by addition of 3-amino-4-(2-methylphenyl)-7,8-dihydrocyclopenta[g][1]benzopyran-2(6H)-one (582 mg) and N,N-dimethylaniline (0.25 ml). The mixture was then stirred at room temperature for 20 hours, after which it was washed with water, dried (MgSO<) and distilled to remove the solvent. The residue was chromatographed on silica gel and eluted with benzeneacetone (9:1) to give 3-(3,4-dimethoxycinnamoylamino)-4-(2-methylphenyl)-7,8-dihydrocyclopenta[g][1]benzopyran-2(6H)-one as oil. The oil was crystallized from ethanol-isopropyl ether (648 mg, 67.4%). Recrystallization from acetone gave colorless needles, m.p. 159°-160° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05264454
출처 데이터셋uspto-grants-1993_11
ORD IDord-eaef6ab8e70d49268db2f8e05d0ad830
출처 메모uspto-grants-1993_11