Dimethylformamide → HCID 18688843, compound
Reaction equation
[Cl:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[C:4]([C:6]1[CH:11]=[C:10](F)[CH:9]=[CH:8][C:7]=1O)=[O:5].[C:18](=[O:21])([O-])[O-].[K+].[K+].Br[CH2:25][C:26]([O:28][CH2:29][CH3:30])=[O:27].[CH3:31]N(C)C=O>>[Cl:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[C:4]([C:6]1[C:18]([O:21][CH2:25][C:26]([O:28][CH2:29][CH3:30])=[O:27])=[C:8]([CH3:7])[CH:9]=[C:10]([CH3:31])[CH:11]=1)=[O:5]Participants
5
Procedure
To a stirred mixture of 1.0 g of compound B and 1.1 g of potassium carbonate in 10 cc of dimethylformamide was added dropwise 0.53 cc of ethyl bromoacetate at room temperature. After the resulting mixture was stirred at room temperature for 16 hours. The insoluble material was filtered off. To the filtrate was added water and ethylacetate and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed three times with a saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was distilled off and the crude product thus obtained was purified by a silica gel column chromatography (eluent: ethyl acetate/hexane=1/4) to obtain 1.06 g of compound C. Yield: 78.7%.
Workup
- filtrationThe insoluble material was filtered off
- additionTo the filtrate was added water and ethylacetate
- extractionthe aqueous layer was extracted with ethyl acetate
- washThe combined organic layer was washed three times with a saturated aqueous sodium chloride solution
- dry with materialdried over magnesium sulfate
- distillationThe solvent was distilled off
- customthe crude product thus obtained
- customwas purified by a silica gel column chromatography (eluent: ethyl acetate/hexane=1/4)
Sources & evidence
- ORD record
- ord-54bd5dac22b14ac9b2a83a4a2c25cc90
- Source dataset
- uspto-grants-1995_11
- Patent number
- US05464863
Reaction notes
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