참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Epichlorohydrin | HCID 7835 | — |
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | Bromomethylcyclopropane | HCID 81503 | — |
| 반응물 | 4-(2-(Cyclopropylmethoxy)ethoxy)-2-methylphenol | HCID 19797594 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Methyl-1-(2,3-epoxypropoxy)-4-(2-(cyclopropylmethoxy)ethoxy)benzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05242943 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-e0f6b927331840ff8925668d568d22be |
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| 출처 메모 | uspto-grants-1993_09 |
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