Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Phosphine | HCID 24404 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Phenylethanol | HCID 7409 | — |
Reaction Steps
Into a 3 ounce glass pressure bottle are placed 180 milligrams of [Rh(norbornadiene) (iso-propylphenylmethylphosphine)2 ]BF4 ([α]D25 = +11.0° for the phosphine), 7.7 grams of acetophenone, 3 ml absolute ethanol, and 0.12 ml water. The bottle is flushed and filled with hydrogen as in Example 1 to 30 psig. The bottle is warmed to 60°C and the contents stirred for 5 hours. Distillation of the reaction mass affords pure α-methylbenzyl alcohol, [α]D25 = -1.78°, optical purity = 4.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03968147 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-51efbe8de474488896d56775330223ba |
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| Source note | uspto-grants-1976_07 |
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