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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70559Generated: October 29, 2026

Water → HCID 67399087, compound

https://huagongshe.com/reaction/70559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-bromo-N-(2-hydroxyethyl)-N-methylbenzenesulfonamideHCID 39403192—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventChloroformHCID 6212—
ProductHCID 67399087HCID 67399087100%

Reaction Steps

A solution of 4-bromo-N-(2-hydroxyethyl)-N-methylbenzenesulfonamide (1.339 g) in chloroform (15 mL) was stirred in an ice bath, during which tert-butyldimethylchlorosilane (1.04 g) and N,N-dimethyl-4-aminopyridine (84 mg) were added thereto. Triethylamine were added dropwise, and the mixture was returned to room temperature and stirred for 16 hours. The reaction solution was poured into water, followed by extraction with chloroform. The organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=95:5→60:40) to give 4-bromo-N-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-N-methylbenzenesulfonamide as a colorless powder (1.77 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822503B2
Source datasetuspto-grants-2014_09
ORD IDord-bced49e2d8c64b8b8db9560ea3be668d
Source noteuspto-grants-2014_09