HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275050Generated: October 26, 2026
P-Toluenesulfonamide → 2-acetamido-2,3-dimethyl-N-(p-tolylsulfonyl)butyramide
https://huagongshe.com/reaction/275050
Participants
| Role | Name | HCID | Charge |
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| Reactant | P-Toluenesulfonamide | HCID 6269 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2-Acetamido-2,3-dimethylbutanoic acid | HCID 233805 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-acetamido-2,3-dimethyl-N-(p-tolylsulfonyl)butyramide | HCID 14624688 | 116.7% |
Reaction Steps
2-Acetamido-2,3-dimethylbutyric acid (1.5 g) is dissolved in a solution of triethylamine (2.7 g) in diethyl ether (50 mL) and cooled to 0° C.; ethylchloroformate (1.1 g) is added dropwise and the mixture is stirred at 0° to room temperature over one hour. The mixture is filtered, and the filtrate is concentrated in vacuo to afford the oily mixed anhydride (1.5 g). This material is mixed with 3 g of p-toluenesulfonamide, sodium salt, in 25 mL dimethylformamide, and the resulting mixture is heated at 80° C. for 16 hours. The reaction is cooled, concentrated in vacuo, and the residue is partitioned between methylene chloride and saturated, aqueous sodium bicarbonate. Acidification of the aqueous layer with conc. HCl to pH 1, extraction with CH2Cl2, drying, and stripping the organic phase affords the title product (3.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05391757 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-459db0b05ded459db5ab4ca5be40b901 |
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| Source note | uspto-grants-1995_02 |
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