Hydrochloric Acid → p-Hydrazinobenzenesulphonamide

HRID 1489338Notes

Reaction equation

HRID 1489338 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH2:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[N:12]([O-])=O.[Na+].Cl>O>[CH:3]1[C:2]([NH:1][NH2:12])=[CH:7][CH:6]=[C:5]([S:8]([NH2:11])(=[O:9])=[O:10])[CH:4]=1

Participants

5

Conditions

Temperature
5 °C

Procedure

4-Aminobenzenesulfonamide (52 g, 0.3 mol) was dissolved in 200 ml H2O containing 30 ml 30% NaOH and added to 75 ml 4N NaNO2. The resulting solution was poured over 100 g crushed ice containing 100 ml 30% HCl at a rate needed to maintain a reaction temperature of 5° C. The diazotization step was carried out for 40 min and the resultant diazonium salt was then added slowly to a stirred solution of 99.95 g Na2 SO3 in 250 ml water at 10° C., and the reaction was continued for 1 h. At this point, the reaction temperature was raised to 70° C. and 300 ml 30% HCl was added over 30 min. The precipitated product was stirred overnight, collected by filtration, washed with cold water and dried. The phenylhydrazine-4-sulfonamide obtained (47 g) was dissolved in 600 ml H2O containing 40 ml 30% NaOH, and to this solution 27.5 g (0.26 mol) of benzaldehyde was added at 50°-55° C. After stirring for 1 h, the temperature was reduced to 30° C. and 24 ml 30% HCl was added. The precipitated product was collected by filtration, washed with cold water and dried, to give 47.2 g of benzaldehyde phenylhydrazone-4-sulfonamide (m.p. 199° C.).

Workup

  1. additionThe resulting solution was poured over 100 g
  2. waitthe reaction was continued for 1 h
  3. temperatureAt this point, the reaction temperature was raised to 70° C.
  4. filtrationcollected by filtration
  5. washwashed with cold water
  6. customdried

Sources & evidence

ORD record
ord-65a55c3150734ec88becd6c87255e75b
Source dataset
uspto-grants-1997_10
Patent number
US05677434

Reaction notes

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