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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36265Generated: October 26, 2026

Tert-Butylamine → N-tert-butyl-4-propylbenzenesulfonamide

https://huagongshe.com/reaction/36265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
Reactant4-N-Propylbenzenesulphonyl chlorideHCID 2737222—
SolventDichloromethaneHCID 6344—
ProductN-tert-butyl-4-propylbenzenesulfonamideHCID 6470063—

Reaction Steps

To a solution of 4-n-propylbenzenesulfonyl chloride (Lancaster) in anhydrous CH2Cl2 (0.5M solution) cooled to 0° C. under N2 was added t-butylamine (2.2 equiv) slowly through a dropping funnel. After complete addition, the reaction was stirred at room temperature for 12 hours. The CH2Cl2 was removed under reduced pressure, and the residue was extracted into ether and washed with 2N NaOH, H2O and brine. The organic phase was dried over anhydrous MgSO4 and concentrated in vacuo to afford the titled product; Rf =0.46 (3:1 hexane-EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411980
Source datasetuspto-grants-1995_05
ORD IDord-ccbebb7318f94b96b6a561d0473d3f04
Source noteuspto-grants-1995_05