Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352397Generated: October 30, 2026

4-Methoxybenzenesulfonyl chloride → HCID 22711751, compound

https://huagongshe.com/reaction/352397

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-2-methyl-1-propanolHCID 11807—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22711751HCID 2271175179.8%

Reaction Steps

Part A: To a solution of 4.47 g (50 mmol) of 2-amino-2-methyl-1-propanol in 20 mL of THF and 5 mL of water, was added 10 mL (72 mmol) of triethylamine. After cooling in an ice bath, 9.0 g (44 mmol) of 4-methoxybenzenesulfonyl chloride was slowly added over 10 minutes. After stirring at room temperature for 12 hours, the reaction was concentrated, ethyl acetate and water were added, the organic layer was separated and washed with 5% potassium hydrogen sulfate solution, saturated sodium bicarbonate solution and brine, dried over sodium sulfate, filtered and concentrated to afford 9.1 g of the desired N-(2-hydroxy-1,1-dimethylethyl)-4-methoxybenzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747027B1
Source datasetuspto-grants-2004_06
ORD IDord-bddfbcd05b854ae8ad832743ae99352d
Source noteuspto-grants-2004_06