HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291900Generated: October 30, 2026
Triethylamine → N-{2-[(Dimethylsulfamoyl)amino]ethyl}acetamide
https://huagongshe.com/reaction/2291900
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(2-aminoethyl)acetamide | HCID 66082 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{2-[(Dimethylsulfamoyl)amino]ethyl}acetamide | HCID 14010264 | — |
Reaction Steps
A solution of 14.3 g (0.1 mole) of dimethylsulfamoyl chloride in 50 ml of methylene chloride was added dropwise to a rapidly stirred solution of 10.2 g (0.1 mole) of acetylethylene diamine and 10.1 g (0.1 mole) of triethylamine in 150 ml of methylene chloride at 25° C. After the addition was completed, the solution was stirred for 30 min and then washed in a separatory funnel with two 100 ml portions of water. The organic phase was separated, and dried over MgSO4, and then concentrated under reduced pressure to afford N-[2[(dimethylamino)sulfonylamino]ethyl]acetamide as an oil. The N-acetyl group was then removed by treatment of the oil with 100 ml of 15% HCl at 80° C. for 6 h. This solution was concentrated under reduced pressure to provide 12.6 g (73%) of product as an oil. The NMR spectrum was consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04798892 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-a547348ffa024297a796d7458d71ffcf |
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| Source note | uspto-grants-1989_01 |
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