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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748925Generated: October 26, 2026

Tert-Butylamine → N-t-Butyl 4-bromobenzenesulfonamide

https://huagongshe.com/reaction/748925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
ReactantTriethylamineHCID 8471—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-t-Butyl 4-bromobenzenesulfonamideHCID 79662986.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Place t-butylamine (4.32 mL, 41.1 mmol), triethylamine (8.15 mL, 58.7 mmol) and dichloromethane (75 mL) in a 3-neck round bottom flask. Cool this stirring solution to 0° C. and add a solution of 4-bromobenzenesulfonyl chloride (10.0 g, 39.1 mmol) in dichloromethane (50 mL). Add additional dichloromethane (25 mL) and stir the reaction overnight, allowing it to warm to ambient temperature. Evaporate the reaction in vacuo. Suspend the resulting white solid in ethyl acetate and filter it. Concentrate the filtrate in vacuo and purify the resulting residue by flash chromatography (silica gel; 50%-80% gradient CH2Cl2 in hexanes) to provide 9.85 g of 4-bromo-N-tert-butyl-benzenesulfonamide (86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399867B2
Source datasetuspto-grants-2008_07
ORD IDord-8d902a682dc54efdb5a5ca7f8fd1df48
Source noteuspto-grants-2008_07