Hydrochloric Acid → 4-[(Thiophen-2-yl)sulfanyl]benzene-1,2-diamine
Reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([S:8][C:9]2[S:10][CH:11]=[CH:12][CH:13]=2)[CH:5]=[CH:4][C:3]=1[N+:14]([O-])=O.Cl>>[NH2:14][C:3]1[CH:4]=[CH:5][C:6]([S:8][C:9]2[S:10][CH:11]=[CH:12][CH:13]=2)=[CH:7][C:2]=1[NH2:1]Participants
3
Procedure
3.3 G. of 2-amino-1-nitro-4-(thien-2-ylthio)benzene is treated with 16 g. stannous chloride in 16 ml. concentrated hydrochloric acid on the steam bath for 5 minutes. The mixture is cooled, decanted and the gummy residue washed with 16 ml. 6N hydrochloric acid. The residue is dissolved in water, and treated with potassium bicarbonate solution and chloroform. The chloroform is dried and stripped yielding 1,2-diamino-4-(thien-2-ylthio)benzene.
Workup
- temperatureThe mixture is cooled
- customdecanted
- washthe gummy residue washed with 16 ml
- dissolutionThe residue is dissolved in water
- additiontreated with potassium bicarbonate solution and chloroform
- dry with materialThe chloroform is dried
Sources & evidence
- ORD record
- ord-8f7e49edcc0e4869b1703d0cb402efc5
- Source dataset
- uspto-grants-1977_01
- Patent number
- US04005202
Reaction notes
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