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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21256생성일: 2026년 10월 25일

Chloromethyl Methyl Ether → 3-Chloro-4-methoxymethoxybenzoic acid

https://huagongshe.com/reaction/21256

반응식

참여 물질

역할이름HCID투입량
반응물Chloromethyl Methyl EtherHCID 7864—
반응물Potassium HydroxideHCID 14797—
반응물3-Chloro-4-hydroxybenzoic acidHCID 19860—
반응물DiisopropylethylamineHCID 81531—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물3-Chloro-4-methoxymethoxybenzoic acidHCID 5798668895.1%

반응 단계

3-Chloro-4-hydroxybenzoic acid 0.5 hydrate (2.00 g, 11.6 mmol) was suspended in dichloromethane (50 mL), and the suspension was added with diisopropylethylamine (8.10 mL, 46.5 mmol) and chloromethyl methyl ether (1.80 mL, 23.7 mmol), under ice-cooling. The reaction mixture was warmed to room temperature and stirred for 1.5 hours. The reaction mixture was added with chloromethyl methyl ether (0.45 mL, 5.92 mmol) under ice-cooling, and stirred at room temperature for 1.5 hours. The reaction mixture was added with methanol (100 mL) and 4 mol/L aqueous potassium hydroxide solution (50 mL) and stirred at room temperature for 18 hours. The solvent was evaporated under reduced pressure, and the residue was added with 4 mol/L hydrochloric acid and water, followed by extracting with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to obtain 3-chloro-4-methoxymethoxybenzoic acid (2.39 g, yield 95%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-98ca684b2d7041bc8d3afabb280632b7
출처 메모uspto-grants-2010_06