Diethyl Oxalate → HCID 12897298, compound
Reaction equation
[C:1]1([NH2:8])[CH:6]=[CH:5][CH:4]=[C:3]([NH2:7])[CH:2]=1.[C:9]([O:16][CH2:17][CH3:18])(=[O:15])[C:10]([O:12]CC)=O>CCOCC>[C:1]1([NH:8][C:10](=[O:12])[C:9]([O:16][CH2:17][CH3:18])=[O:15])[CH:6]=[CH:5][CH:4]=[C:3]([NH:7][C:10](=[O:12])[C:9]([O:16][CH2:17][CH3:18])=[O:15])[CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of m-phenylenediamine (10.8 grams) 0.10 ml.) and diethyl oxalate (50 ml.) is refluxed for 2.5 hours. The cooled reaction mixture is diluted with ether (200 ml.) and the crude product collected (19.2 grams, M.P. 150° C.). Two recrystallizations from methanol give off white crystals (6.65 grams, 155°-160° ).
Workup
- customThe cooled reaction mixture
- customthe crude product collected (19.2 grams, M.P. 150° C.)
- customTwo recrystallizations from methanol
- customgive off white crystals (6.65 grams, 155°-160° )
Sources & evidence
- ORD record
- ord-8154c8ed532b4f888459635b9eef2372
- Source dataset
- uspto-grants-1978_05
- Patent number
- US04089973
Reaction notes
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