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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233381생성일: 2026년 10월 26일

Water → 4-(2',3'-Dimethoxyphenyl) 3-phenylbutyric acid

https://huagongshe.com/reaction/233381

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium HydroxideHCID 14798—
반응물4-(2',3'-Dimethoxyphenyl)-3-phenylbutanenitrileHCID 19961101—
용매EthanolHCID 702—
생성물4-(2',3'-Dimethoxyphenyl) 3-phenylbutyric acidHCID 1247854398%

반응 단계

4-(2',3'-Dimethoxyphenyl)-3-phenylbutanenitrile (20 g, 71 mmol), from Step 4, was dissolved in 1.5 L of ethanol. Sodium hydroxide (20 g, 0.5 mol) and 200 mL of water were added and the reaction mixture was heated at reflux temperature for 24 h. The solvent was removed in vacuo and 1 L of water plus 1 L of methylene chloride were added to the residue. The layers were separated and the organic layer discarded. The aqueous layer was acidified with concentrated hydrochloric acid and extracted with 3 L of ethyl acetate. The ethyl acetate solution was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to give 21 g (98% yield) of the title compound as an oil; 1H NMR (CDCl3) δ: 2.6-2.7 (m, 2H), 2.9 (d, 2H), 3.4-3.5 (m, 1H), 3.72 (s, 3H), 3.82 (s, 3H), 6.6 (dd, 1H), 6.73 (dd, 1H), 6.88 (t, 1H), 7.1-7.3 (m, 5H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591884
출처 데이터셋uspto-grants-1997_01
ORD IDord-de20507ff9aa4d49828923c54aec8c2b
출처 메모uspto-grants-1997_01