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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15061생성일: 2026년 10월 24일

Chloromethyl Methyl Ether → 4-Fluoro-3-(methoxymethoxy)benzyl alcohol

https://huagongshe.com/ko/reaction/15061

반응식

참여 물질

역할이름HCID투입량
반응물Chloromethyl Methyl EtherHCID 7864—
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물4-Fluoro-3-hydroxybenzoic acidHCID 593635—
용매Ethyl AcetateHCID 8857—
생성물4-Fluoro-3-(methoxymethoxy)benzyl alcoholHCID 2307431194%

반응 조건

온도0 °C

반응 단계

Triethylamine (1.07 mL) and methoxymethyl chloride (2.24 mL) were added to tetrahydrofuran (10 mL) solution of 4-fluoro-3-hydroxybenzoic acid (1.0 g), and stirred at 0° C. for 2 hours. Ethyl acetate was added to the reaction liquid which then was washed with water and saturated brine, dried over anhydrous magnesium sulfate, the solvent therein was concentrated under reduced pressure and the residue was dissolved in tetrahydrofuran (20 mL). Lithiumaluminium hydride (360 mg) was added, stirred at 0° C. for an hour, ethyl acetate was added and the insoluble matter was removed, followed by washing with saturated brine and drying over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the title compound (1.14 g, 94%) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732456B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b32e232e6caf496cb7414acd838cedd1
출처 메모uspto-grants-2010_06