Sulfuric Acid → 4-Hydrazinobenzenesulfonic acid

HRID 1489339Notes

Reaction equation

HRID 1489339 reaction equation
[S:1]([OH:11])(=[O:10])([C:3]1[CH:8]=[CH:7][C:6]([NH2:9])=[CH:5][CH:4]=1)=[O:2].OS(O)(=O)=O.[N:17]([O-])=O.[Na+]>O>[CH:7]1[C:6]([NH:9][NH2:17])=[CH:5][CH:4]=[C:3]([S:1]([OH:11])(=[O:10])=[O:2])[CH:8]=1

Participants

5

Conditions

Temperature
10 °C

Procedure

Sulfanilic acid (52 g, 0.3 mol) was dissolved in 200 ml H2O containing 16.5 g Na2CO3. The resulting solution was cooled to 10° C. and 35 g of conc. H2SO4 was then added dropwise, followed by the addition of 75 ml 4N NaNO2. The diazotization step was carried out for 15 min at 10°-12° C., then the diazonium salt was collected by filtration, washed with a small amount of cold water and added, at 5° C., to a stirred solution of 85 g of Na2 SO3 in 250 ml H2O. After stirring the reaction mixture for 1 h, the temperature was raised to 95° C. and 240 ml of concentrated H2SO4 was added over a period of 30 min. The reaction mixture was left overnight and the precipitated product was collected, washed with cold water and dried. The phenylhydrazine-4-sulfonic acid obtained (52 g) was dissolved in 500 ml H2O containing 60 ml 30% NaOH, and 30 g (0.28 mol) of benzaldehyde was added at 50°-55° C. Stirring was continued for 1 h, the temperature was reduced to 30° C., and the product was precipitated by acidification with 36 ml 30% HCl. The product was collected, washed with a small amount of cold water and dried, to give 50 g of benzaldehyde phenylhydrazone-4-sulfonic acid.

Workup

  1. filtrationthe diazonium salt was collected by filtration
  2. washwashed with a small amount of cold water
  3. additionadded, at 5° C., to a stirred solution of 85 g of Na2 SO3 in 250 ml H2O
  4. temperaturethe temperature was raised to 95° C.
  5. addition240 ml of concentrated H2SO4 was added over a period of 30 min
  6. waitThe reaction mixture was left overnight
  7. customthe precipitated product was collected
  8. washwashed with cold water
  9. customdried

Sources & evidence

ORD record
ord-d43f351e28bf490f91004c1bffbf1b15
Source dataset
uspto-grants-1997_10
Patent number
US05677434

Reaction notes

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