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 0.5M 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 3N 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 | US05021460 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-51fb0e7bbc244d4696a9614e3f2252da |
| Source note | uspto-grants-1991_06 |