Hydrochloric Acid → HCID 10657374, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([O:8][C:9]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][CH:10]=2)[CH:5]=[CH:4][C:3]=1[N+:16]([O-])=O.Cl>>[NH2:16][C:3]1[CH:4]=[CH:5][C:6]([O:8][C:9]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][CH:10]=2)=[CH:7][C:2]=1[NH2:1]Participants
3
Procedure
1.2 G. of 2-amino-4-(p-chlorophenoxy)-1-nitrobenzene in 3 ml. concentrated hydrochloric acid is treated with a solution of 6 g. stannous chloride in 6 ml. concentrated hydrochloric acid on the steam bath for 5 minutes. The mixture is cooled, decanted and the residue washed with 6 ml. 6N hydrochloric acid. The residue is treated with potassium bicarbonate and chloroform, filtered, and the chloroform layer repeated and dried over magnesium sulfate. Evaporation leaves 1,2-diamino-4-(p-chlorophenoxy)-benzene as a gum.
Workup
- temperatureThe mixture is cooled
- customdecanted
- washthe residue washed with 6 ml
- additionThe residue is treated with potassium bicarbonate and chloroform
- filtrationfiltered
- dry with materialdried over magnesium sulfate
- customEvaporation
Sources & evidence
- ORD record
- ord-93393df5bf4b47419253a9152ed57789
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03965113
Reaction notes
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