Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Phenylethanol, (S)- | HCID 443135 | — |
Reaction Steps
Under nitrogen stream, acetophenone (20 mmol), RuCl[(S)-xylbinap][(S)-daipen] (1/100 molar fold of acetophenone) and t-BuOK (5 molar folds of the ruthenium catalyst) were added to a Schlenk tube. 2-propanol (8.3 mL per 100 mg of acetophenone) was added, then stirred for 10 minutes at 30° C. As a result of analysis of the reaction mixture by gas chromatography (Chirasil-DEX CB), it was found that the conversion rate is 94%, and the optical purity is 98.4% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079931B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-1e9c3a54f4b54e6189ca860d34bd05d2 |
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| Source note | uspto-grants-2015_07 |
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