Pyrazole → 2-Chloro-4-(1-pyrazolyl)methylphenyl 2,2-dimethylpropanoate
Reaction equation
[NH:1]1[CH:5]=[CH:4][CH:3]=[N:2]1.[H-].[Na+].[H][H].[CH3:10][C:11]([CH3:25])([CH3:24])[C:12]([O:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21]Br)=[CH:17][C:16]=1[Cl:23])=[O:13]>CN(C)C=O>[CH3:10][C:11]([CH3:25])([CH3:24])[C:12]([O:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][N:1]2[CH:5]=[CH:4][CH:3]=[N:2]2)=[CH:17][C:16]=1[Cl:23])=[O:13]Participants
Conditions
- Temperature
- 10 °C
Procedure
A mixture of pyrazole (15.3 g), sodium hydride (60%, 8.99 g) and anhydrous N,N-dimethylformamide (200 ml) was stirred at 60° to 70° C. under a nitrogen atmosphere for 2 hours. After the evolution of hydrogen gas ceased, the mixture was cooled to 10° C. To this mixture was added dropwise an anhydrous N,N-dimethylformamide (300 ml) solution of 4-bromomethyl-2-chlorophenyl 2,2-dimethylpropanoate (68 g) at room temperature under stirring over 1 hour, and the mixture was stirred at 80° C. for 1 hour. After cooling, the reaction mixture was poured into ice water, which was extracted with ethyl acetate. The organic layer was washed with saturated aqueous ammonium chloride solution and then saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, which afforded 39.5 g of 2-chloro-4-(1-pyrazolyl)methylphenyl 2,2-dimethylpropanoate as a colorless oil. Yield, 60%.
Workup
- stirringunder stirring over 1 hour
- stirringthe mixture was stirred at 80° C. for 1 hour
- temperatureAfter cooling
- extractionwas extracted with ethyl acetate
- washThe organic layer was washed with saturated aqueous ammonium chloride solution
- dry with materialsaturated sodium chloride solution, dried with anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-680b8bd8f74d401aa5c6d7a672f5df22
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05684022
Reaction notes
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