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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29692생성일: 2026년 10월 24일

3-(4-Phenylphenyl)prop-2-enoic acid → HCID 69208772, 화합물

https://huagongshe.com/ko/reaction/29692

반응식

참여 물질

역할이름HCID투입량
반응물3-(4-Phenylphenyl)prop-2-enoic acidHCID 25492—
반응물Sodium BicarbonateHCID 516892—
반응물HCID 57419527HCID 57419527—
용매AcetoneHCID 180—
용매Thionyl ChlorideHCID 24386—
생성물HCID 69208772HCID 6920877279.2%

반응 단계

A mixture of 3-biphenyl-4-yl-acrylic acid (0.449 g, 2.004 mmol) in SOCl2 (5 ml) was refluxed for 2 h. After cooling, the solvent was removed. The residue was dissolved in acetone and added into a stirred solution of 4-hydroxy-2-(naphthoylamino)-benzoic acid methyl ester (0.335 g, 2.004 mmol) in acetone (10 ml) with NaHCO3 (0.202 g, 2.405 mmol). After 18 h, the reaction mixture was concentrated. The residue was triturated with water, filtered and the solids rinsed with ether and dried to give 2-{[(2E)-3-(1,1′-biphenyl-4-yl)prop-2-enoyl]amino}-4-hydroxybenzoic acid methyl ester (0.593 g, 1.588 mmol, 79%) as an off-white solid, mp 292-296° C. 1H NMR (DMSO-d6) δ 3.88 (s, 3H), 6.57 (dd, 1H), 6.95 (d, 1H), 7.37-7.54 (m, 3H), 7.67 (d, 1H), 7.70-7.80 (m, 4H), 7.80-7.90 (m, 3H), 8.20 (dd, 1H), 10.55 (s, 1H), 11.20 (s, 1H); mass spectrum [ES(−)], m/z 372 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420083B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-fc4d352f78474d82a83dbd78f5fdcee5
출처 메모uspto-grants-2008_09