HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzyl Alcohol → Benzyl 8-bromooctanoate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzyl Alcohol | HCID 244 | — |
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | 8-Bromooctanoic acid | HCID 548275 | — |
| Katalysator | 4-Pyrrolidinopyridine | HCID 75567 | — |
| Lösungsmittel | Carbon Tetrachloride | HCID 5943 | — |
| Produkt | Benzyl 8-bromooctanoate | HCID 11278409 | — |
Reaktionsschritte
There were dissolved 11.6 g (52 mmol) of 8-bromooctanoic acid in 100 ml of CCl4 and around 5° C. (ice bath), there were added to the solution 5.41 g (50 mmol) of benzyl alcohol and 2.5 mmol of 4-pyrrolidino-pyridine catalyst. Thereafter, a solution of 10.73 g (52 mmol) of dicyclohexylcarbodiimide (DCC) in 10 ml of carbon tetrachloride was added portion-wise under stirring. The precipitation of the expected dicyclohexylurea (DCU) was effective after a few min and the temperature was allowed to come back to room temperature. After ½ hr, the reaction was complete as checked by TLC (hexane/ether 1:1). Then after about 1 hr, 0.5 ml of AcOH were added to quench remaining DCC and the DCU was filtered out after about one hour (yield 11.2 g=100%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06706280B2 |
| Quelldatensatz | uspto-grants-2004_03 |
| ORD ID | ord-3f77a10e74bf44d4b323cf8ea0e05ff6 |
| Quellennotiz | uspto-grants-2004_03 |