Reaction equation
[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][CH:4]([CH3:8])[CH:3]1[OH:9].CC1CCCC(C)C1=O>>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[OH:9]Participants
3
Procedure
Using a procedure similar to that described in Example 2, 100 g/hour of a mixture consisting of 50% by weight of 2,6-dimethylcyclohexanol and 50% by weight of 2,6-dimethylcyclohexanone were converted, at 250° C. and under otherwise identical conditions, over the catalyst described in the stated example. This procedure gave 2,6-dimethylphenol in a yield of 97% of theory.
Workup
- customwere converted, at 250° C. and under otherwise identical conditions, over the catalyst
Sources & evidence
- ORD record
- ord-bac1fac11fe54627a8d631b3e47d65e5
- Source dataset
- uspto-grants-1985_08
- Patent number
- US04538009
Linked notes
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