Acetic Acid → HCID 22165514, compound
Reaction equation
[N+](=[CH:3][C:4](=[O:9])[CH2:5][CH2:6][CH:7]=[CH2:8])=[N-].[C:10]([OH:13])(=[O:12])[CH3:11]>>[C:10]([O:13][CH2:3][C:4](=[O:9])[CH2:5][CH2:6][CH:7]=[CH2:8])(=[O:12])[CH3:11]Participants
3
Procedure
Into 35 ml of glacial acetic acid at 60°-70° C. is dropped slowly 12.4 g. (0.1 mole) of 1-diazo-5-hexen-2-one. After the nitrogen evolution stops, the reaction mixture is heated to reflux for one hour. The resulting mixture is extracted with 3×50 ml of methylene chloride. The organic layer is dried over anhydrous magnesium sulfate. Concentration of the filtrate gives 1-acetoxy-5-hexen-2-one as a brown oil in 90% yield, based on the starting 4-pentenoyl chloride. ##STR40##
Workup
- temperaturethe reaction mixture is heated
- temperatureto reflux for one hour
- extractionThe resulting mixture is extracted with 3×50 ml of methylene chloride
- dry with materialThe organic layer is dried over anhydrous magnesium sulfate
Sources & evidence
- ORD record
- ord-c864f4295d864270b81429b32da1cfd3
- Source dataset
- uspto-grants-1980_10
- Patent number
- US04226866
Reaction notes
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