HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → 1-Phenyl-1-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| 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
12.2 mg (2×10-5 moles) of [Ir(PPEI)COD]+ClO4- (+) were suspended in 50 ml of isopropanol and oxidized with air for 4 hours. The yellow limpid solution so obtained was degasified for 20 minutes at reflux under a nitrogen stream and then treated with 2.7 ml of a deaerated isopropanol solution of KOH (2 mg of KOH). The solution was preliminarily reduced for 30 minutes in a N2 stream at reflux and then treated with 2.56 ml of deaerated propiophenone. After 60 minutes the reaction was stopped, obtaining a conversion to phenylpropanol (+) of 57.3% with an e.e. of 30%. Ratios:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04290961 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-9e73c4547a364ebbb8239f5e056fb5cd |
| Source note | uspto-grants-1981_09 |