Water → 4-(2,3-Dihydro-2,2-dimethylbenzofuran-7-ylmethyl)cyclohexanone
Reaction equation
[CH3:1][C:2]1([CH3:22])[CH2:6][C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([CH2:11][CH:12]3[CH2:21][CH2:20][C:15]4(OCC[O:16]4)[CH2:14][CH2:13]3)[C:4]=2[O:3]1.O>C(O)(=O)C>[CH3:1][C:2]1([CH3:22])[CH2:6][C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([CH2:11][CH:12]3[CH2:21][CH2:20][C:15](=[O:16])[CH2:14][CH2:13]3)[C:4]=2[O:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
This compound is prepared in a manner analogous to that of Step D of Example 2, using 5.4 grams (0.018 mole) of 8-(2,3-dihydro-2,2-dimethylbenzofuran-7-ylmethyl)-1,4-dioxaspiro[4.5]decane and 25 mL of water in 100 mL of acetic acid, yielding 4-(2,3-dihydro-2,2-dimethylbenzofuran-7-ylmethyl)cyclohexanone.
Workup
- customThis compound is prepared in a manner analogous to that of Step D of Example 2
Sources & evidence
- ORD record
- ord-7218c90dc3144e66a6f5c4cb5f2f9e90
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05536725
Reaction notes
Loading…