HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenyl-1-propanone → 1-Phenyl-1-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenyl-1-propanone | HCID 7148 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Perchlorate | HCID 123351 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Phenyl-1-propanol | HCID 7147 | — |
Reaction Steps
6.1 mg (1×10-5 moles) of [Ir(PPEI)COD]+ClO4- (+) were suspended in 50 ml of isopropanol and oxidized with air for 4 hours. The yellow solution obtained was then degasified at reflux in a nitrogen stream for 20 minutes and then treated with 4.0 ml of an isopropanol solution of KOH (4 mg of KOH). The solution, after a preliminary reduction for 30 minutes at reflux in a nitrogen flow, was treated with 2.56 ml of deaerated propiophenone. After 180 minutes, a conversion to phenylpropanol (+) of 89.3% with an e.e. of 26.1% was obtained. Ratios:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04290961 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-3f4fa818b9204438a89165bb7a56f984 |
| Source note | uspto-grants-1981_09 |