Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | sodium 2-methylpropan-2-olate | HCID 178418730 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Phenylethanol | HCID 7409 | — |
Reaction Steps
Into a 100-mL stainless-steel autoclave was put 24.0 mg (0.03 mmol) of [CuCl((R,R)-SKEWPHOS) (PPh3)]n obtained in Example 27, triphenyl phosphine of the amount shown in Table 6 below, and 28.8 mg (0.30 mmol) of NaO-t-Bu, followed by replacing with nitrogen in the autoclave, and then 2.0 mL of isopropyl alcohol and 1.05 mL (9.0 mmol) of acetophenone were added. The reaction was carried out with stirring under a hydrogen pressure of 5 MPa at 30° C. for 16 to 17 hours to give 1-phenethyl alcohol which is a hydrogenated compound of acetophenone. The reaction mixture was analyzed by using GC. The results are shown in Table 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902110B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-0fb5e6c50cb749a6887872802e3a3df6 |
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| Source note | uspto-grants-2011_03 |
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