HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
p-Toluenesulfonic acid → 4-Propyl-cyclohexanecarboxylic acid 4-acryloyloxy-butyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 4-Hydroxybutyl acrylate | HCID 75588 | — |
| Edukt | (1s,4r)-4-Propylcyclohexane-1-carboxylic acid | HCID 1490324 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4-Propyl-cyclohexanecarboxylic acid 4-acryloyloxy-butyl ester | HCID 59289090 | — |
Reaktionsschritte
4-Propyl-cyclohexanecarboxylic acid (10.0 g, 58.0 mmol), 4-hydroxybutyl acrylate (8.0 g, 57.0 mmol) and a catalytic amount of para-toluene sulphonic acid are stirred under reflux in toluene (100 ml) in a flask equipped with Dean-Stark apparatus. The reaction is shown to be complete by GCMS after 1 hour. The solution is allowed to cool to room temperature, is washed with aqueous sodium carbonate and water, dried and evaporated to dryness. Purification is achieved by flash column chromatography using petrol as eluant. Evaporation of the appropriate fractions gives a colourless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08372307B2 |
| Quelldatensatz | uspto-grants-2013_02 |
| ORD ID | ord-a2e30c497dba4744a6945527d75788a1 |
| Quellennotiz | uspto-grants-2013_02 |