Hydrochloric Acid → HCID 10823051, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([CH2:8][CH3:9])[C:5]([Cl:10])=[CH:4][C:3]=1[NH2:11].[C:12](O)(=[O:16])[C:13](O)=[O:14].Cl>>[Cl:10][C:5]1[CH:4]=[C:3]2[C:2](=[CH:7][C:6]=1[CH2:8][CH3:9])[NH:1][C:13](=[O:14])[C:12](=[O:16])[NH:11]2Participants
4
Procedure
A mixture of 1,2-diamino-4-chloro-5-ethylbenzene (from (a), 2.70 g, ca 13 mmol), oxalic acid (1.65 g, 18.3 mmol) and 4M hydrochloric acid (66 ml) was heated at reflux for 4.6 h, cooled, and the grey solid collected by filtration and washed with water. The solid was dried in vacuo at 50° C. to afford the title compound (2.34 g, 80%), m.p. >315° C.
Workup
- temperaturewas heated
- temperatureat reflux for 4.6 h
- temperaturecooled
- filtrationthe grey solid collected by filtration
- washwashed with water
- customThe solid was dried in vacuo at 50° C.
Sources & evidence
- ORD record
- ord-f85c5462d7b44737aa8461e07e6429b2
- Source dataset
- uspto-grants-1998_12
- Patent number
- US05852016
Reaction notes
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