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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1822253생성일: 2026년 10월 26일

Cesium carbonate → 3-{4-[3-(4-Chloro-2-cyclohexyl-phenoxy)-5-methyl-phenoxy]-2-methyl-phenyl}-propionic acid

https://huagongshe.com/reaction/1822253

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Sodium HydroxideHCID 14798—
반응물2,2,6,6-Tetramethyl-3,5-heptanedioneHCID 70700—
반응물4-Chloro-2-cyclohexylphenolHCID 83120—
반응물3-[4-(3-Bromo-5-methyl-phenoxy)-2-methyl-phenyl]-propionic acid methyl esterHCID 57894212—
촉매Cuprous chlorideHCID 62652—
용매MethanolHCID 887—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물3-{4-[3-(4-Chloro-2-cyclohexyl-phenoxy)-5-methyl-phenoxy]-2-methyl-phenyl}-propionic acidHCID 1120241538%

반응 단계

A solution of 3-[4-(3-bromo-5-methyl-phenoxy)-2-methyl-phenyl]-propionic acid methyl ester (0.1 g, 0.27 mmol), 4-chloro-2-cyclohexyl-phenol (63 mg, 0.3 mmol), copper(I) chloride (13 mg, 0.13 mmol), 2,2,6,6-tetramethyl-3,5-heptanedione (0.01 mL, 0.07 mmol), and cesium carbonate (105 mg, 0.32 mmol) in NMP (3 mL) is heated to 120° C. The reaction is stirred overnight and cooled to rt. The reaction is quenched with 1N aqueous HCl and extracted with ethyl ether. The organic layer is washed with brine, dried over sodium sulfate, and filtered. The solvent is removed to afford the crude ester intermediate. The intermediate is treated with 5N NaOH (0.4 mL, 2.2 mmol) in MeOH (5 mL) and heated to reflux. The reaction stirred at reflux for 2 hours and then cooled. The reaction is quenched with 1N aqueous HCl to obtain pH=4. The aqueous layer is extracted with ethyl ether. The organic layer is washed with brine, dried over sodium sulfate, and filtered. The solvent is removed to afford the crude product. The crude is purified by HPLC to afford 49 mg (38%) of desired product. 1H NMR (400 MHz, CDCl3); MS (ES+) m/z mass calculated for C29H31ClO4 478, found 479 and 481 (M+1 and M+3, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07608639B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-e510c01daf424293b294850e22a1f045
출처 메모uspto-grants-2009_10