Reaktionsgleichung
[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][CH2:11][C:12]([OH:14])=O)[CH2:6][CH2:5]1)(=[O:3])[CH3:2].S(Cl)([Cl:17])=O>>[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][CH2:11][C:12]([Cl:17])=[O:14])[CH2:6][CH2:5]1)(=[O:3])[CH3:2]Komponenten
3
Versuchsvorschrift
To 100 ml of thionyl chloride was added 26 g of 3-(1-acetylpiperidin-4-yl)propionic acid, obtained in Reference Example 1-(2), in small portions with ice-cooling. The mixture was stirred for 5 minutes, after which the excess thionyl chloride was distilled off and the solid residue was washed with diethyl ether to give 26.4 g of 3-(1-acetylpiperidin-4-yl)propionyl chloride as a pale yellow powder.
Aufarbeitung
- temperaturein small portions with ice-cooling
- distillationafter which the excess thionyl chloride was distilled off
- washthe solid residue was washed with diethyl ether
Quellen und Nachweise
- ORD-Eintrag
- ord-d878f7c71dea4699bd97b412d55dc53e
- Quelldatensatz
- uspto-grants-1993_12
- Patentnummer
- US05273974
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