Dimethylformamide → (Cyclohex-1-en-1-yl)(2,3-dichloro-4-methoxyphenyl)methanone
Reaction equation
[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([O:9][CH3:10])[CH:5]=[CH:4][C:3]=1[C:11]([C:13]1(Br)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)=[O:12].[Cl-].[Li+].CN(C)C=O>O>[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([O:9][CH3:10])[CH:5]=[CH:4][C:3]=1[C:11]([C:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH:14]=1)=[O:12]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1-Bromocyclohexyl (2,3-dichloro-4-methoxyphenyl) ketone (47.3 g., 0.13 mole), lithium chloride (16.5 g., 0.39 mole) and dimethylformamide (200 ml.) are heated at 90°C. for two hours, then poured into water (1 l.) to give 36.5 g. of 1-cyclohexenyl (2,3-dichloro-4 -methoxyphenyl) ketone which melts at 126°-129°C. after drying at 60°C. under vacuum for 16 hours.
Workup
- customto give 36.5 g
- dry with materialof 1-cyclohexenyl (2,3-dichloro-4 -methoxyphenyl) ketone which melts at 126°-129°C. after drying at 60°C. under vacuum for 16 hours
Sources & evidence
- ORD record
- ord-bdd8ac3ca41d4d86bd4f3518aeac1739
- Source dataset
- uspto-grants-1976_08
- Patent number
- US03976686
Reaction notes
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