6-(Benzyloxy)-3,3-dimethyl-2,3-dihydrobenzofuran → 3,3-Dimethyl-2,3-dihydro-1-benzofuran-6-ol
Reaction equation
C([O:8][C:9]1[CH:19]=[CH:18][C:12]2[C:13]([CH3:17])([CH3:16])[CH2:14][O:15][C:11]=2[CH:10]=1)C1C=CC=CC=1.[H][H]>CO.[Pd]>[CH3:16][C:13]1([CH3:17])[C:12]2[CH:18]=[CH:19][C:9]([OH:8])=[CH:10][C:11]=2[O:15][CH2:14]1Participants
5
Procedure
To a solution of 6-(benzyloxy)-3,3-dimethyl-2,3-dihydrobenzofuran (3.48 g, 13.7 mmol) in methanol (200 mL) was added Pd/C (1.45 g) and the mixture was hydrogenated under 40 psi of hydrogen overnight. 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, 1/7) to give the title compound (1.66 g, 74%): MS (ES+) m/z 165.4 (M+1).
Workup
- filtrationThe reaction mixture was filtered through celite
- washwashed with methanol
- concentrationThe filtrate was concentrated in vacuo to dryness
Sources & evidence
- ORD record
- ord-017cc2ac5ef742859ae239559dcbe71e
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07700641B2
Reaction notes
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