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 (0.01 8 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-27cb1879436e4a4fb8e3f7d869f23017
- Source dataset
- uspto-grants-1998_01
- Patent number
- US05712281
Reaction notes
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