HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 729009Erstellt: 23. Oktober 2026
Tetrahydrofuran → 2-Methyl-1-(2,3-epoxypropoxy)-4-(2-(cyclopropylmethoxy)ethoxy)benzene
https://huagongshe.com/de/reaction/729009
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | Bromomethylcyclopropane | HCID 81503 | — |
| Edukt | 4-(2-(Cyclopropylmethoxy)ethoxy)-2-methylphenol | HCID 19797594 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Produkt | 2-Methyl-1-(2,3-epoxypropoxy)-4-(2-(cyclopropylmethoxy)ethoxy)benzene | HCID 19797587 | — |
Reaktionsschritte
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 withepichlorhydrin 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)).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05051445 |
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| Quelldatensatz | uspto-grants-1991_09 |
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| ORD ID | ord-f08186d9065347379c741da11d868b7d |
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| Quellennotiz | uspto-grants-1991_09 |
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