HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(benzyloxy)-2,2-dimethylbenzofuran-3(2H)-one → 2,2-Dimethyl-2,3-dihydrobenzofuran-6-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(benzyloxy)-2,2-dimethylbenzofuran-3(2H)-one | HCID 66642518 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,2-Dimethyl-2,3-dihydrobenzofuran-6-ol | HCID 20037293 | 88% |
Reaction Steps
To a solution of 6-(benzyloxy)-2,2-dimethylbenzofuran-3(2H)-one (0.85 g, 3.20 mmol) in methanol (100 mL) was added palladium hydroxide (0.22 g, 20 wt. % loading, 0.32 mmol). The resulting mixture was hydrogenated for 16 hours under 60 psi of hydrogen. The reaction mixture was filtered through celite, washed with methanol. The filtrate was concentrated in vacuo to dryness. The residue was subjected to column chromatography (ethyl acetate/hexane, 1/5) to give the title compound (0.46 g, 88%): 1H NMR (300 MHz, CDCl3) δ 6.92 (d, 1H), 6.30-6.21 (m, 2H), 4.77 (s, 1H), 2.90 (s, 2H), 1.44 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106087B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-d34809e02a3d470a87bd329c46487e67 |
| Source note | uspto-grants-2012_01 |