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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29691생성일: 2026년 10월 24일

Potassium Hydroxide → 3-(4-Phenylphenyl)prop-2-enoic acid

https://huagongshe.com/ko/reaction/29691

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물3-Biphenyl-4-yl-acrylic acid methyl esterHCID 69208604—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물3-(4-Phenylphenyl)prop-2-enoic acidHCID 2549284%

반응 단계

To a suspension of 3-biphenyl-4-yl-acrylic acid methyl ester (9.384 g, 39.38 mmol) in THF (120 ml) and MeOH (80 ml) was added 1N KOH (79 ml) and the mixture refluxed. After 3 h, heating was stopped. The reaction mixture was concentrated to about 50 ml, diluted with water (200 ml) and acidified with 2N HCl (80 ml). EtOAc (1000 ml) was added and the whole mixture heated to boiling to dissolve all solids. After cooling, the layers were separated and the organic layer washed with 1N HCl (2×70 ml), water (3×70 ml), brine (2×50 ml), dried over Na2SO4, filtered, concentrated and dried to give 3-biphenyl-4-yl-acrylic acid (7.393 g, 32.966 mmol, 84%) as a white solid, dec. 223-226° C. 1H NMR (DMSO-d6) δ 6.58 (d, 1H), 7.37-7.53 (m, 3H), 7.62 (d, 1H), 7.70-7.84 (m, 6H), 12.40 (s, 1H); mass spectrum [ES(−)], m/z 223 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420083B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-8a6ec0d1cadf4067844245e9ccae4d46
출처 메모uspto-grants-2008_09