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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 229241생성일: 2026년 10월 25일

Methanol → 4-(3-Methoxy-3-oxopropyl)benzoic acid

https://huagongshe.com/reaction/229241

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Thionyl ChlorideHCID 24386—
반응물3-(4-Carboxyphenyl)propionic AcidHCID 854054—
생성물4-(3-Methoxy-3-oxopropyl)benzoic acidHCID 1131029484%

반응 단계

To a suspension of 3-(4-carboxyphenyl)propionic acid (2.0 g, 10.1 mmol) in methanol (20 mL) was added thionyl chloride (38 μL, 0.50 mmol). The reaction mixture was stirred at room temperature for 16 h, and a clear solution was obtained. The solvent was removed under reduced pressure. The residue was taken up in ether (100 mL), washed with saturated aqueous NaHCO3 (2×50 mL) and water (50 mL). The combined NaHCO3 and water extract was acidified with concentrated HCl in an ice bath. The precipitated white solid was collected, washed with water and dried to yield 1.76 g (84%) of compound 166 as off-white solid. The material was used without further purification. mp 146-148° C. 1H NMR (400 MHz, CDCl3): δ 2.66 (t, J=7.7 Hz, 2H), 3.02 (t, J=7.7 Hz, 2H), 3.67 (s, 3H), 7.30 (d, J=8.3 Hz, 2H), 8.03 (d, J=8.1 Hz, 2H). LCMS (ES), m/z, 209 (M+H)+, 207 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560589B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-d08b68924eba4f69bfb540bae1614219
출처 메모uspto-grants-2009_07