Epichlorohydrin → 2-Methyl-4-(2,3-epoxypropoxy)benzaldehyde
Reaktionsgleichung
[CH2:1]([CH:3]1[O:5][CH2:4]1)Cl.[CH3:6][C:7]1[CH:14]=[C:13]([OH:15])[CH:12]=[CH:11][C:8]=1[CH:9]=[O:10].CC1C=C(CC2OC2)C=CC=1C=O>[OH-].[Na+]>[CH3:6][C:7]1[CH:14]=[C:13]([O:15][CH2:1][CH:3]2[O:5][CH2:4]2)[CH:12]=[CH:11][C:8]=1[CH:9]=[O:10]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 55 °C
Versuchsvorschrift
To epichlorohydrin (20 g., 0.216 mole) heated at 55° C. is added dropwise a solution of 2-methyl-4-hydroxybenzaldehyde (9.0 g., 0.006 mole) in 2.5 N sodium hydroxide solution (40 ml.). After the addition, the solution is allowed to stir an additional 3 hours at 55° C. and then at room temperature overnight. the oil is distilled to give 8.3 g. of 2-methyl-4-(2,3-epoxypropyl)benzaldehyde, m.p. 160°-170° C. at 1 mm. Hg.
Aufarbeitung
- additionAfter the addition
- customat room temperature
- customovernight
- distillationthe oil is distilled
- customto give 8.3 g
Quellen und Nachweise
- ORD-Eintrag
- ord-ca0230d404b140aeafd5657131abbb71
- Quelldatensatz
- uspto-grants-1989_08
- Patentnummer
- US04853383
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