HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(2-iodophenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-Chloro-2-iodoaniline | HCID 2757615 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-iodophenyl)methanesulfonamide | HCID 780001 | 111.1% |
Reaction Steps
To the mixture of the 2-iodo-4-chloroaniline (5.0 g, 20 mmol) and triethylamine (8.3 mL, 60 mmol) in methylene chloride (200 mL), the solution of methanesulfonyl chloride (3.4 mL, 44 mmol) was added slowly. The solution then was stirred at room temperature for 2 h. After being washed by HCl solution (0.5 N, 2×100 mL), NaOH solution (0.5 N, 2×100 mL), brine (100 mL), the organic layer was dried over Na2SO4 and concentrated providing the title compound (6.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06872834B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-e4dcb3a2d8e34a1780f1edc9a4bc0fa2 |
| Source note | uspto-grants-2005_03 |