Sodium Hydroxide → HCID 70618826, compound
Reaction equation
[N:1]1[C:6]([C:7]2[CH:11]=[C:10]([C:12]([O:14]CC)=[O:13])[O:9][N:8]=2)=[CH:5][CH:4]=[CH:3][C:2]=1[C:17]1[CH:21]=[C:20]([C:22]([O:24]CC)=[O:23])[O:19][N:18]=1.[OH-].[Na+]>O>[OH2:9].[N:1]1[C:2]([C:17]2[CH:21]=[C:20]([C:22]([OH:24])=[O:23])[O:19][N:18]=2)=[CH:3][CH:4]=[CH:5][C:6]=1[C:7]1[CH:11]=[C:10]([C:12]([OH:14])=[O:13])[O:9][N:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 2.5 g. (0.005 mole) of diethyl 3,3'-(2,6-pyridinediyl)di-5-isoxazolecarboxylate and 250 mg. of sodium hydroxide in 50 ml. of water is refluxed for ninety minutes. The reaction mixture is cooled to room temperature and the insoluble material removed by filtration. The filtrate is acidified with concentrated hydrochloric acid. The gelatinous precipitate is removed by filtration and washed with water. There is obtained 610 mg. of a tan solid (38%) melting at 284° (dec.).
Workup
- additionA mixture of 2.5 g
- customthe insoluble material removed by filtration
- customThe gelatinous precipitate is removed by filtration
- washwashed with water
- customThere is obtained 610 mg
Sources & evidence
- ORD record
- ord-99ba83b161a04d4296cda77777a3e9f5
- Source dataset
- uspto-grants-1978_01
- Patent number
- US04066769
Reaction notes
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