Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Product | 1-Phenylethanol, (R)- | HCID 637516 | 92.1% |
Reaction Steps
To the reaction solution obtained in (3) were added acetophenone (0.56 ml, 4.81 mmol) and 2-propanol (9.4 ml, 121 mmol), and the mixture was stirred at 25° C. for 24 hours. The reaction mixture was purified by means of Kugelrohr distillation to give (R)-1-phenylethanol (0.541 g, 92% yield). The asymmetric yield of the product was measured in a HPLC using a CHIRALCEL OD column (4.6×250 mm, Daicel Chemical Industries Ltd) and found to be not less than 99% e.e. In the table below, the results obtained by using a metal-ligand complex 4 (described on page 9800 of J. Am. Chem. Soc. 1993, 115, 9800-9801 and hereinafter referred to as the comparative compound) are also given for comparison.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07635776B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-51eb4be6ae58423dbbb4c31184aeefdd |
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| Source note | uspto-grants-2009_12 |
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