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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892944Generated: October 26, 2026

P-Toluenesulfonamide → 2-acetamido-2,3-dimethyl-N-(p-tolylsulfonyl)butyramide

https://huagongshe.com/reaction/892944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ToluenesulfonamideHCID 6269—
ReactantEthyl chloroformateHCID 10928—
Reactant2-Acetamido-2,3-dimethylbutanoic acidHCID 233805—
ReactantSodiumHCID 5360545—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product2-acetamido-2,3-dimethyl-N-(p-tolylsulfonyl)butyramideHCID 14624688116.7%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120854
Source datasetuspto-grants-1992_06
ORD IDord-1aaf1bd93ac045f2967f1539737bd5ad
Source noteuspto-grants-1992_06