HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731721Generated: October 29, 2026
Hydrochloric Acid → 2-[(4-Butylphenyl)sulfamoyl]benzoic acid
https://huagongshe.com/reaction/1731721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20226978 | HCID 20226978 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[(4-Butylphenyl)sulfamoyl]benzoic acid | HCID 15597024 | — |
Reaction Steps
Reaction scheme II is carried out by slowing adding the cooled reaction mixture into a 4 liter beaker containing 250 ml water and 300 ml of hydrochloric acid (37%), and equipped with an efficient stirrer, taking care that the mixture does not foam over. The dispersion is chilled in a refrigerator over night. The crude N-(p-n-butylphenyl)-o-carbomethoxy benzene sulfonamide settles on the bottom of the beaker as a brownish, viscous mass. The water layer is poured off and replaced by a solution of 80 g sodium hydroxide in 1.5 liter of water. The resulting solution is heated for 2 hours at 85° C. to hydrolize the methyl ester (reaction scheme III). ##STR39##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04623391 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-393d89685c5b47a08f70cb0067c4b96f |
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| Source note | uspto-grants-1986_11 |
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