Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18617849 | HCID 18617849 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18617820 | HCID 18617820 | — |
Reaction Steps
To a cooled solution (0° C.) of 2-[4-(1,1-dimethyl-allyl)-phenyl]-furan (424 mg, 2 mmol) (reference example 51)in THF (4 mL) is added dropwise (1M)borane-THF complex (2.2 mL, 2.2 mmol) and the resulting mixture stirred for 1 hour. To the mixture is added 10% NaOH (1.5 mL) and 30 wt % H2O2 (1.5 mL) and stirred for 1 hour while allowing to warm to 20° C. The mixture is diluted with ether, washed with water and brine, dried over MgSO4 and concentrated. The residue is purified by flash chromatography (eluting with 25% ethyl acetate in hexanes) to give 341 mg of the title compound. 1H NMR (CDCl3) δ 1.34 (s, 6H), 1.40 (m, 1H), 1.94 (t, J=8 Hz, 2H), 3.48 (t, J=8 Hz, 2H), 6.45 (m, 1H), 6.60 (m, 1H), 7.35 (d, J=8 Hz, 2H), 7.44 (bs, 1H), 6.61 (d, J=8 Hz, 2H). MS (EI) m/z 230 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06541505B1 |
|---|
| Source dataset | uspto-grants-2003_04 |
|---|
| ORD ID | ord-c9ca72576ebc4163868c1012ab5f8cd0 |
|---|
| Source note | uspto-grants-2003_04 |
|---|