HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463330Generated: October 27, 2026
Triethylamine → N-(4-nitrobenzyl)methanesulfonamide
https://huagongshe.com/reaction/1463330
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-Nitrobenzylamine hydrochloride | HCID 11252467 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-nitrobenzyl)methanesulfonamide | HCID 12822520 | 85% |
Reaction Steps
To a solution of 25.0 g (133 mmol, 1.0 equiv.) of 4-nitro benzylamine hydrochloride in 500 mL of methylene chloride at 0° C. was added 46.4 mL (331 mmol, 2.5 equiv.) of triethylamine followed by 11.3 mL (146 mmol, 1.1 equiv.) of methanesulfonyl chloride dropwise. The reaction was stirred for thirty minutes at 0° C. then diluted with 500 mL of chloroform. The organic layer was washed with 150 mL portions of 1N HCl and saturated sodium chloride. The organic layer was dried over magnesium sulfate, filtered and concentrated to give 25.8 g (85%) of N-[(4-nitrophenyl)methyl]methanesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05300506 |
|---|
| Source dataset | uspto-grants-1994_04 |
|---|
| ORD ID | ord-edd256646853408ca89f6d014932bad0 |
|---|
| Source note | uspto-grants-1994_04 |
|---|