HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-bromo-N-methylbenzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | m-Bromobenzenesulphonyl chloride | HCID 17943 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-bromo-N-methylbenzene-1-sulfonamide | HCID 7213265 | 90% |
Reaction Steps
Methylamine hydrochloride (1057 mg, 15.65 mmol) and triethylamine (3.3 mL, 23.48 mmol) were dissolved in dichloromethane (20 mL) and then 3-bromobenzene-1-sulfonyl chloride (4.0 g, 15.65 mmol) was slowly added. The reaction mixture was stirred at room temperature for 2 hours, diluted with dichloromethane, and washed with brine. The organic layer was dried with magnesium sulfate, filtered with celite, and then concentrated. The resultant target compound (3.5 g, 90% yield) was used in the following reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586580B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-61980d8ba9bb430d919dada04c5d25b4 |
| Source note | uspto-grants-2013_11 |