Potassium Iodide → Cyclohexanone, 2,2-dimethyl-6-(phenylmethylene)-
Reaction equation
[OH-].[K+].[I-].[K+].[CH3:5][CH:6]1[CH2:11][CH2:10][CH2:9][C:8](=[CH:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:7]1=[O:19].[CH3:20]Cl>C(O)(C)(C)C>[CH3:5][C:6]1([CH3:20])[CH2:11][CH2:10][CH2:9][C:8](=[CH:12][C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[C:7]1=[O:19]Participants
Procedure
66 g of 85% strength potassium hydroxide solution and 750 ml of tert-butanol were placed in a 1 l 4-necked flask, and the mixture was heated briefly at reflux with stirring. Then 8.3 g of potassium iodide were added, the mixture was cooled to room temperature and 200 g of 2-methyl-6-benzylidene-cyclohexanone were added. 101 g of methyl chloride were passed in at room temperature over 8 hours. The mixture was subsequently stirred at room temperature for 8 hours, and then 450 ml of tert-butanol were distilled off. 500 ml of water were added to the residue, the mixture was stirred thoroughly, and the product which separates out was filtered off with suction. Recrystallization from methanol gave 161 g (75% of theory) of pure product with a melting point of 79°-81° C.,
Workup
- temperaturethe mixture was heated briefly
- temperatureat reflux
- stirringThe mixture was subsequently stirred at room temperature for 8 hours
- distillation450 ml of tert-butanol were distilled off
- addition500 ml of water were added to the residue
- stirringthe mixture was stirred thoroughly
- filtrationthe product which separates out was filtered off with suction
- customRecrystallization from methanol
- customgave 161 g (75% of theory) of pure product with a melting point of 79°-81° C.
Sources & evidence
- ORD record
- ord-0a1324ce3e584f83b007e0c4c15f4a8e
- Source dataset
- uspto-grants-1997_09
- Patent number
- US05663447
Reaction notes
Loading…