Hydrochloric Acid → 1-(2-Hydroxy-4,6-dimethylphenyl)-1-butanone
Reaction equation
C([O:6][C:7]1[CH:12]=[C:11]([CH3:13])[CH:10]=[C:9]([CH3:14])[CH:8]=1)(=O)CCC.[Cl-].[Al+3].[Cl-].[Cl-].Cl>>[C:7]([C:12]1[C:11]([CH3:13])=[CH:10][C:9]([CH3:14])=[CH:8][C:7]=1[OH:6])(=[O:6])[CH2:8][CH2:9][CH3:10]Participants
4
Conditions
- Temperature
- 70 °C
Procedure
180 g. of 1-butyryloxy-3,5-dimethyl-benzene are treated at room temperature with 340 g. of aluminium chloride. The mixture is stirred for 4 hours at 90°-95° C., then cooled at 70° C., poured onto ice and 3n aqueous hydrochloric acid and extracted with ether. The ether extract is washed with water to neutral reaction, dried over sodium sulfate and evaporated. There is obtained 2-butyryl-3,5-dimethyl-phenol, which melts at 48°-52° C. after recrystallization from petroleum ether.
Workup
- extractionextracted with ether
- extractionThe ether extract
- washis washed with water to neutral reaction
- dry with materialdried over sodium sulfate
- customevaporated
Sources & evidence
- ORD record
- ord-8e8bbcf8810c4ca2b4a0126498923e40
- Source dataset
- uspto-grants-1987_04
- Patent number
- US04656310
Reaction notes
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