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HCID 13860722, compound → 4-(Benzenesulfonyl)benzene-1,2-diamine

HRID 1679451
Notes
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Reaction equation

HRID 1679451 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([S:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)(=[O:10])=[O:9])[CH:5]=[CH:4][C:3]=1[N+:17]([O-])=O.[H][H]>CO.[Ni]>[NH2:17][C:3]1[CH:4]=[CH:5][C:6]([S:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)(=[O:10])=[O:9])=[CH:7][C:2]=1[NH2:1]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 13860722HCID 13860722, compoundHCID 178418361HCID 178418361, compound

Product 1

HCID 138607234-(Benzenesulfonyl)benzene-1,2-diamine

Reagents, catalysts & solvents 2

HCID 935NickelCatalystHCID 887MethanolSolvent

Procedure

1.9 g. of 2-amino-1-nitro-4-phenylsulfonylbenzene is treated in methanol with hydrogen at 4 atmospheres in the presence of Raney nickel catalyst for 2 hours. The catalyst if filtered off and the filtrate stripped under vacuum. Recrystallization of the residue gives 1,2-diamino-4-phenylsulfonylbenzene.

Workup

  1. filtrationThe catalyst if filtered off
  2. customRecrystallization of the residue

Sources & evidence

ORD record
ord-06cfadf0517d4487af378fe1981ae19e
Source dataset
uspto-grants-1978_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04080461

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes