HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → 1-Phenylethanol, (R)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Phenylethanol, (R)- | HCID 637516 | 99.6% |
Reaction Steps
Acetophenone (200 ml, 1.5 mol) was charged to the catalyst solution, followed by 2-propanol (0.5 l). The pressure was reduced (28.5 mmHg) and then a sodium 2-propoxide solution (120 ml of 0.1M solution in 2-propanol) was charged. The mixture was stirred at ambient temperature under nitrogen for 2.5 h, at hourly intervals the flask was back filled with nitrogen and sufficient 2-propanol charged to compensate for the volume removed by distillation. This gave (R)-1-phenylethanol Yield 99.6%, ee 82.9%. The turnover number, integrated over 1 h, was 454 h−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06372931B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-18b5ceca610c458da7e6883b7b9bfcec |
| Source note | uspto-grants-2002_04 |