HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → 5-p-t-Butylphenoxy-1-pentanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-tert-Butyl-4-[(pent-4-en-1-yl)oxy]benzene | HCID 13313733 | — |
| Reactant | HCID 178418648 | HCID 178418648 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-p-t-Butylphenoxy-1-pentanol | HCID 13313734 | — |
Reaction Steps
The 5-(p-tert-butylphenoxy)-1-pentene (10.5 g) was treated with 115 ml 0.5 M 9-borabicyclononane in tetrahydrofuran and the reaction mixture was stirred at reflux for one hour. The solution was cooled to room temperature and treated with 25 ml 3 N sodium hydroxide, then 10 ml 30% hydrogen peroxide. After the bubbling ceased the reaction mixture was partitioned between 150 ml ether-150 ml water. The ether layer was removed, dried (MgSO4), and evaporated to a yellow oil which was chromatographed through 300 g, 90 to 200 mesh silica gel (2% MeOH/CH2Cl2 eluent) yielding a yellow oil which was vacuum distilled (126° C./0.75 mm) to a clear, colorless oil, 5-p-t-butylphenoxy-1-pentanol, 1.7 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04451474 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-e485f6188cd64cb78a794474e6a2fe60 |
| Source note | uspto-grants-1984_05 |