p-Toluenesulfonic acid → Cyclopentyl-2-mercaptopropionate
Reaktionsgleichung
[CH:1]1([OH:6])[CH2:5][CH2:4][CH2:3][CH2:2]1.[SH:7][CH:8]([CH3:12])[C:9](O)=[O:10].C1(C)C=CC(S(O)(=O)=O)=CC=1>C(OCC)C>[CH:1]1([O:6][C:9](=[O:10])[CH:8]([SH:7])[CH3:12])[CH2:5][CH2:4][CH2:3][CH2:2]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Into a 250 ml reaction flask equipped with stirrer, thermometer, reflux condenser and heating mantle are placed 86 grams of cyclopentanol; 25 grams of 2-mercaptopropionic acid; and 1 gram of paratoluene sulfonic acid. The reaction mass is heated to reflux and refluxed for a period of 8 hours. At the end of the 8 hour reflux period, the reaction mass is cooled and admixed with 200 ml diethylether followed by washing with two 100 ml volumes of 10% aqueous sodium carbonate and one 100 ml volume of water. The reaction mass is dried over anhydrous sodium sulfate and the solvent is recovered on a Buchi apparatus. The reaction mass is then micro distilled yielding the product having the structure: ##STR134##
Aufarbeitung
- customInto a 250 ml reaction flask
- customequipped with stirrer
- temperaturethermometer, reflux condenser
- temperatureheating mantle
- temperatureThe reaction mass is heated
- temperatureto reflux
- temperaturerefluxed for a period of 8 hours
- temperatureAt the end of the 8 hour reflux period
- temperaturethe reaction mass is cooled
- washby washing with two 100 ml volumes of 10% aqueous sodium carbonate and one 100 ml volume of water
- dry with materialThe reaction mass is dried over anhydrous sodium sulfate
- customthe solvent is recovered on a Buchi apparatus
- distillationThe reaction mass is then micro distilled
- customyielding the product
Quellen und Nachweise
- ORD-Eintrag
- ord-66a81a8cb5da4cc093fa3f8c32b90fff
- Quelldatensatz
- uspto-grants-1987_03
- Patentnummer
- US04652670
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