HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → 1-Phenylethanol, (R)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Phenylethanol, (R)- | HCID 637516 | 93.6% |
Reaction Steps
An autoclave was charged with acetophenone (1.03 Kg), isopropanol (300 g), and KOH (100 g, 10 M). Catalyst R-XylPPhos RuCl2 R-DAIPEN (150 g) was then added, and the reaction mixture was hydrogenated at a pressure of 30 bar and a temperature of 70° C. for 12 hours. The resultant mixture was transferred into a separatory funnel The aqueous layer was discarded. The organic layer was washed with water (200 ml) and distilled first at 100 mmHg to remove isopropanol, and then at 5-10 mmHg to provide (R)-alpha-methylbenzyl alcohol (980 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08506943B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-40e4fd49c56340ef973c5857ab4a9173 |
| Source note | uspto-grants-2013_08 |