Potassium Hydroxide → HCID 23699128, compound
Reaction equation
[OH-].[K+:2].[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[O:11][C:12]([C:21]3[O:22][CH:23]=[CH:24][CH:25]=3)=[C:13]([CH2:15][C:16]([O:18]CC)=[O:17])[N:14]=2)=[CH:6][CH:5]=1>CO>[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[O:11][C:12]([C:21]3[O:22][CH:23]=[CH:24][CH:25]=3)=[C:13]([CH2:15][C:16]([O-:18])=[O:17])[N:14]=2)=[CH:6][CH:5]=1.[K+:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 0.4 g of potassium hydroxide in 30 ml of methanol is added to 1.0 g of ethyl 2-[2-(4-chlorophenyl)-5-(2-furyl)-4-oxazolyl]acetate at 5° to 10° C. The mixture is stirred at room temperature for 10 hours. Then, the precipitates are collected by filtration, washed with ether and then dried. 0.85 g of potassium 2-[2-(4-chlorophenyl)-5-(2-furyl)-4-oxazolyl]acetate is obtained. Yield: 80.2%
Workup
- filtrationThen, the precipitates are collected by filtration
- washwashed with ether
- customdried
Sources & evidence
- ORD record
- ord-79503de5d6a34a75a1079102c373133d
- Source dataset
- uspto-grants-1987_02
- Patent number
- US04642313
Reaction notes
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