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Ammonia → HCID 21506029, compound

HRID 918622
Notes
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Reaction equation

HRID 918622 reaction equation
[Cl:1][C:2]1[CH:24]=[CH:23][C:5]([NH:6][C:7]2[C:15]([S:16](=[O:19])(=[O:18])[NH2:17])=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[CH:9][C:8]=2[N+:20]([O-])=O)=[CH:4][CH:3]=1.N.S(S([O-])=O)([O-])=O.[Na+].[Na+]>O>[NH2:20][C:8]1[CH:9]=[C:10]([CH:14]=[C:15]([S:16](=[O:18])(=[O:19])[NH2:17])[C:7]=1[NH:6][C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:24][CH:23]=1)[C:11]([OH:13])=[O:12]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 222AmmoniaHCID 24489Sodium DithioniteHCID 21506081HCID 21506081, compound

Product 1

HCID 21506029HCID 21506029, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent2×

Conditions

Temperature
25 °C

Procedure

A mixture of 4-(p-chloroanilino)-3-nitro-5-sulphamyl-benzoic acid (7.43 g), water (50 ml), and concentrated aqueous ammonia (15 ml) was stirred at 25°C, and a solution of sodium dithionite (13.5 g) in water (50 ml) was added dropwise. After 1 hour, the pH of the reaction mixture was adjusted to 2.5, and the precipitated reaction product was filtered off. After repeated recrystallizations from aqueous ethanol, and after drying for 4 hours in vacuo, 3-amino-4-(p-chloroanilino)-5-sulphamyl-benzoic acid was obtained with a melting point of 273°-274°C.

Workup

  1. customthe precipitated reaction product
  2. filtrationwas filtered off
  3. customrecrystallizations from aqueous ethanol
  4. customafter drying for 4 hours in vacuo

Sources & evidence

ORD record
ord-a7dd797aa3c047f7b012a8e6fd671e43
Source dataset
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US03971819

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes