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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548730Generated: October 27, 2026

2,4-Difluorobenzenesulfonyl Chloride → N-(2-{[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}ethyl)-2,4-difluoro-N-methylbenzenesulfonamide

https://huagongshe.com/reaction/548730

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Difluorobenzenesulfonyl ChlorideHCID 2734273—
ReactantN-(2-(tert-Butyldimethylsilyloxy)ethyl)methylamineHCID 16203640—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
ProductN-(2-{[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}ethyl)-2,4-difluoro-N-methylbenzenesulfonamideHCID 5766320540.7%

Reaction Steps

2,4-Difluorobenzenesulfonyl chloride (1 g, 4.70 mmol) in DCM (2 mL) was added slowly to a solution of (2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)methylamine (980 mg, 5.17 mmol) in DCM (65 mL) and 10% sodium hydroxide solution (65 mL) at 0° C. The reaction was allowed to warm to RT and stirred for 20 hours. The DCM layer was separated and the aqueous re-extracted into DCM (2×50 mL). The combined organics were washed with brine (80 mL), dried (MgSO4), and reduced in vacuo to give the desired compound as a colourless oil (0.7 g). 1H NMR δ (CDCl3): 0.00 (s, 6H), 0.83 (s, 9H), 2.91 (s, 3H), 3.24 (t, 2H), 3.73 (t, 2H), 6.87-6.96 (m, 2H), 7.82-7.88 (m, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943607B2
Source datasetuspto-grants-2011_05
ORD IDord-0e5d01cc5a474f6c8d717c6ecfa1abfb
Source noteuspto-grants-2011_05