HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387569Generated: October 31, 2026
Benzenesulfonyl chloride → HCID 21715919, compound
https://huagongshe.com/reaction/1387569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 3-Amino-4-methoxybenzanilide | HCID 8426 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21715919 | HCID 21715919 | — |
Reaction Steps
A mixture of 3-amino-4-methoxy-N-phenyl-benzamide (0.9726 g, 4.00 mmol), triethylamine (0.56 mL, 4.02 mmol), and benzenesulfonyl chloride (0.51 mL, 4.00 mmol) in ethyl acetate (70 mL) was heated briefly to obtain a solution. The reaction was stirred overnight at room temperature under nitrogen. An additional equivalent of triethylamine and 1/2 equivalent of benzenesulfonyl chloride was added and the mixture heated to 50-60° C. After 7 hours, the solvent was removed in vacuo and the residue dissolved in ethyl acetate and washed with 1N HCl followed by saturated NaHCO3. The organic layer was filtered, dried with MgSO4, and stripped of solvent by rotary evaporator. Trituration of the residue in hexane/ethyl acetate (4:1) afforded the product (0.268 g); m.p. 190-194° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06268387B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-87b391f93cc340368e1fdfa2a8da9ea4 |
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| Source note | uspto-grants-2001_07 |
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