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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065094Generated: November 3, 2026

Sulfanilic acid → HCID 12852926, compound

https://huagongshe.com/reaction/1065094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfanilic acidHCID 8479—
Reactant4-(Bromomethyl)benzophenoneHCID 122951—
ReactantSodium Acetate TrihydrateHCID 23665404—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 12852926HCID 1285292654.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a 1-liter 3-necked round-bottomed flask equipped with overhead stirrer, reflux condenser, dropping funnel and thermometer and containing a stirred slurry of 33.8 g (0.195 mole) of sulfanilic acid in 150 ml of warm (60° C.) water was added 55 g (0.404 mole) of sodium acetate trihydrate and 50 ml of acetonitrile. The resulting yellow solution was heated to 70° C. and a solution of 35 g (0.127 mole) of the 4-(bromomethyl)benzophenone prepared above in 80 ml of acetonitrile was added dropwise over 11/2 hrs. The resulting solution was then refluxed for 5 hrs. Approximately 75 ml of acetonitrile was then removed by distillation at the same time that a dropwise addition of 32 ml of conc. HCl (over a 20 minute period) was made. The mixture was then vacuum filtered at 80° C. which gave a pale yellow powder. The powder was then slurried in 250 ml of water for 15 minutes and again isolated by vacuum filtration. The resulting solids were reslurried in 250 ml of methanol and isolated by vacuum filtration which afforded 25.28 g (54.2%) of purified 4-(((4-benzoylphenyl)methyl)amino)benzenesulfonic acid as a pale yellow powder, which decomposed at 257°-259° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04328244
Source datasetuspto-grants-1982_05
ORD IDord-f53eff30c1b144b6a795b941f72eb50b
Source noteuspto-grants-1982_05