HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344185Generated: October 25, 2026
Benzenesulfonamide → HCID 15104381, compound
https://huagongshe.com/reaction/344185
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 4110026 | HCID 4110026 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium chloride ethyl acetate | HCID 86643102 | — |
| Product | HCID 15104381 | HCID 15104381 | — |
Reaction Steps
960 mg (2.5 mmol) of 4'-[(2-n-butyl-benzimidazol-1-yl)-methyl]biphenyl-2-carboxylic acid are dissolved in 25 ml of methylene chloride, treated with 2 ml of thionyl chloride and heated under reflux for one hour. The solvent is then distilled off and evaporated 2 times after adding methylene chloride. 390 mg (2.5 mmol) of benzenesulphonamide are added to the residue and the mixture is heated for one hour at 140° C. After cooling, the oil obtained is taken up in ethyl acetate/sodium chloride solution and extracted 3 times using ethyl acetate. The combined ethyl acetate phases are dried over sodium sulphate, evaporated and the crude product obtained is purified over a silica gel column using methylene chloride/ethanol as eluting agent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05864043 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-62db22f44978472f964c5b6bd9136ec7 |
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| Source note | uspto-grants-1999_01 |
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