Toluene → 1-Naphthol
Reaction equation
[OH2:1].[C:2]1([CH3:12])[CH:7]=[CH:6][C:5](S(O)(=O)=O)=[CH:4][CH:3]=1.[C:13]1([CH3:19])C=CC=C[CH:14]=1>>[CH:5]1[CH:4]=[CH:3][C:2]2[C:7](=[CH:14][CH:13]=[CH:19][C:12]=2[OH:1])[CH:6]=1Participants
3
Conditions
- Temperature
- 90 °C
Procedure
The compound of the above formula (33) was dissolved in 120 ml of toluene and heated to 90° C. 57.6 g (303.0 mmol) of p-toluenesulfonic acid monohydrate was added to this solution and refluxed for 4 hours. After the reaction, the reaction product was washed in water, the solvent was removed, and the obtained product was purified by column chromatography to obtain a naphthol compound represented by the following formula (34) as 4.4 g (7.6 mmol, yield rate of 75%) of a white solid.
Workup
- temperaturerefluxed for 4 hours
- customAfter the reaction
- washthe reaction product was washed in water
- customthe solvent was removed
- customthe obtained product was purified by column chromatography
Sources & evidence
- ORD record
- ord-ca03c67687e043cca70b7bb2683a23f7
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08691120B2
Reaction notes
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