HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (E)-4-Chloro-2-(2-(3,4-dichlorophenyl)vinylsulfonamido)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-4-chlorobenzenesulphonamide | HCID 77790 | — |
| Reactant | (E)-2-(3,4-dichlorophenyl)ethenesulfonyl chloride | HCID 22719686 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (E)-4-Chloro-2-(2-(3,4-dichlorophenyl)vinylsulfonamido)benzenesulfonamide | HCID 57750903 | 91.5% |
Reaction Steps
2-Amino-4-chlorobenzenesulfonamide (100 mg, 0.48 mmol) and (E)-2-(3,4-dichlorophenyl)ethenesulfonyl chloride (171 mg, 0.63 mmol) were dissolved in anhydrous dichloromethane (5 mL) and were flushed with argon. Anhydrous triethylamine (0.155 mL, 1.11 mmol) was added and the reaction was stirred at room temperature under an inert atmosphere over night. The reaction was quenched using 2 M hydrochloric acid (20 mL) and extracted with dichloromethane. The combined organic phases were washed with water, dried over magnesium sulfate and concentrated under vacuum to give 194 mg (91% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145380B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-bd24960907dd4c8485d631ba43c33bd7 |
| Source note | uspto-grants-2015_09 |