Hydrochloric Acid → HCID 12897326, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10](=[O:16])[C:11]([O:13]CC)=[O:12])=[CH:5][C:4]=1[NH:17][C:18](=[O:24])[C:19]([O:21]CC)=[O:20].Cl>[OH-].[Na+].O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10](=[O:16])[C:11]([OH:13])=[O:12])=[CH:5][C:4]=1[NH:17][C:18](=[O:24])[C:19]([OH:21])=[O:20]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Diethyl 4-methoxy-N,N'-(m-phenylene)dioxamate (1.0 gm., 0.0029 mole) is stirred in 1.0 N NaOH (10 ml.) at room temperature for one hour, then heated at reflux for thirty minutes. The reaction mixture is diluted with water (25 ml.) and the pH adjusted to 3 with hydrochloric acid. The resulting solid is collected and washed with acetone (0.72 gm., 86%, m.p. >320° ).
Workup
- temperatureheated
- temperatureat reflux for thirty minutes
- customThe resulting solid is collected
- washwashed with acetone (0.72 gm., 86%, m.p. >320° )
Sources & evidence
- ORD record
- ord-be87b53bbe964e4f97187afc27fed694
- Source dataset
- uspto-grants-1979_06
- Patent number
- US04159278
Reaction notes
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