Ethylene Glycol → 3-[3-(1,3-Dioxolan-2-yl)phenoxy]propanamine
Reaktionsgleichung
[CH:1]([C:3]1[CH:4]=[C:5]([CH:21]=[CH:22][CH:23]=1)[O:6][CH2:7][CH2:8][CH2:9][N:10]1C(=O)C2C(=CC=CC=2)C1=O)=[O:2].[CH2:24](O)[CH2:25][OH:26]>C1C=CC=CC=1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>[O:26]1[CH2:25][CH2:24][O:2][CH:1]1[C:3]1[CH:4]=[C:5]([CH:21]=[CH:22][CH:23]=1)[O:6][CH2:7][CH2:8][CH2:9][NH2:10]Komponenten
5
Versuchsvorschrift
A solution of 2-[3-(3-formylphenoxy)propyl]-1H-isoindole-1,3-(2H)-dione (90 g) and p-toluenesulphonic acid, monohydrate (200 mg) in benzene (900 ml) and ethane-1,2-diol (25 g) was heated under reflux using a Dean-Stark separator for 8 h. The cooled solution was washed successively with sodium carbonate solution, water, sodium chloride solution, and evaporated in vacuo. The resulting oil was dissolved in tetrahydrofuran (1 liter) and stirred with hydrazine hydrate (50 ml) at room temperature for 24 hr. The mixture was diluted with ether and filtered. The filtrate was distilled to give the title compound as a colourless oil (55.2 g) b.p. 134°-6° (0.7 mm). TLC silica; methanol:ammonia 80:1; Rf 0.4.
Aufarbeitung
- temperatureunder reflux
- customfor 8 h
- washThe cooled solution was washed successively with sodium carbonate solution, water, sodium chloride solution
- customevaporated in vacuo
- dissolutionThe resulting oil was dissolved in tetrahydrofuran (1 liter)
- additionThe mixture was diluted with ether
- filtrationfiltered
- distillationThe filtrate was distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-def86e0895e9498a9071a9f3791cb42f
- Quelldatensatz
- uspto-grants-1984_04
- Patentnummer
- US04442110
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