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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5017생성일: 2026년 10월 23일

Epichlorohydrin → 2-Methyl-1-(2,3-epoxypropoxy)-4-(2-(cyclopropylmethoxy)ethoxy)benzene

https://huagongshe.com/ko/reaction/5017

반응식

참여 물질

역할이름HCID투입량
반응물EpichlorohydrinHCID 7835—
반응물PiperidineHCID 8082—
반응물BromomethylcyclopropaneHCID 81503—
반응물4-(2-(Cyclopropylmethoxy)ethoxy)-2-methylphenolHCID 19797594—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물2-Methyl-1-(2,3-epoxypropoxy)-4-(2-(cyclopropylmethoxy)ethoxy)benzeneHCID 19797587—

반응 단계

The epoxide starting material is obtained from reaction of 4-hydroxy-3-methylphenyl benzoate with benzyl bromide to give 4-benzyloxy-3-methylphenyl benzoate (M.P. 120°-121° from methanol/ether), followed by de-esterification with 2M NaOH solution to give 4-benzyloxy-3-methylphenol (M.P. 69°-70° from ether/hexane) and reaction with 2-bromoethanol (light brown oil) to form an alcohol which is reacted with cyclopropylmethyl bromide in tetrahydrofuran. Debenzylation of the cyclopropylmethoxyethoxy derivative (unpurified) with 10% Pd on activated charcoal forms 4-(2-(cyclopropylmethoxy)ethoxy)-2-methylphenol which is then reacted with epichlorhydrin in the presence of a catalytic amount of piperidine to give 2-methyl-1-(2,3-epoxypropoxy)-4-(2-(cyclopropylmethoxy)ethoxy)benzene (light brown oil after chromatography on silica gel with toluene/ethyl-acetate (8:2)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05242943
출처 데이터셋uspto-grants-1993_09
ORD IDord-e0f6b927331840ff8925668d568d22be
출처 메모uspto-grants-1993_09