Methanol → Methyl 4-(oxiran-2-yl)butanoate
Reaktionsgleichung
Br[CH2:2][CH:3]1[O:7][C:6](=[O:8])[CH2:5][CH2:4]1.[CH3:9][O-:10].[Na+].[CH3:12]O>O>[CH3:12][O:7][C:6]([CH2:5][CH2:4][CH2:3][CH:2]1[O:10][CH2:9]1)=[O:8]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
10.0 g 4,5-dihydro-5-bromomethyl-(3H)-furanone are refluxed with 3.0 g sodium methylate in 37 ml methanol for 5 hours. The solvent is eliminated in vacuum and the residue is dissolved in 20 ml H2O and then extracted with ether. The ethereal phase is dried through a molecular sieve and the ether eliminated in vacuum. The residue is distilled at 20 mm. 6.4 g 4,5-epoxypentane carboxylic acid methyl ester (boiling point at 20 mm, 85° C.) is obtained.
Aufarbeitung
- extractionextracted with ether
- customThe ethereal phase is dried through a molecular sieve
- distillationThe residue is distilled at 20 mm
Quellen und Nachweise
- ORD-Eintrag
- ord-ec0153c58b604e3794c437fe8ec91fe3
- Quelldatensatz
- uspto-grants-1985_12
- Patentnummer
- US04562270
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