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HRID 5017作成日:2026年10月23日

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

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反応式

関与物質

役割名称HCID仕込み量
反応物EpichlorohydrinHCID 7835—
反応物PiperidineHCID 8082—
反応物BromomethylcyclopropaneHCID 81503—
反応物4-(2-(Cyclopropylmethoxy)ethoxy)-2-methylphenolHCID 19797594—
触媒PalladiumHCID 23938—
溶媒TetrahydrofuranHCID 8028—
生成物2-Methyl-1-(2,3-epoxypropoxy)-4-(2-(cyclopropylmethoxy)ethoxy)benzeneHCID 19797587—

反応手順

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)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05242943
出典データセットuspto-grants-1993_09
ORD IDord-e0f6b927331840ff8925668d568d22be
出典メモuspto-grants-1993_09