Acetic Anhydride → 3-Methyl-4-acetoxybenzofuran
Reaktionsgleichung
[CH3:1][C:2]1[C:6]2[C:7]([OH:11])=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][CH:3]=1.[C:12](OC(=O)C)(=[O:14])[CH3:13].C(N(CC)CC)C>O1CCCC1>[CH3:1][C:2]1[C:6]2[C:7]([O:11][C:12](=[O:14])[CH3:13])=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][CH:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 3-methyl-4-hydroxybenzofuran (5.0 gm, 34.7 mmoles), acetic anhydride (50 mL) and triethylamine (25 mL) in tetrahydrofuran (150 mL) was stirred at room temperature overnight. The volatiles were removed in vacuo and the residue was purified by chromatography on silica gel. Elution with 15% ethylacetate in hexane yielded 3-methyl-4-acetoxybenzofuran.
Aufarbeitung
- customThe volatiles were removed in vacuo
- customthe residue was purified by chromatography on silica gel
- washElution with 15% ethylacetate in hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-1b21741b5e734ad4acd38b85fcc73a3a
- Quelldatensatz
- uspto-grants-1992_02
- Patentnummer
- US05087638
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