Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347352Generated: October 26, 2026

Water → 4-acetyl-N-(tert-butyldimethylsiloxy)benzenesulfonamide

https://huagongshe.com/reaction/347352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Acetylbenzenesulfonyl chlorideHCID 266418—
ReactantO-(tert-Butyldimethylsilyl)hydroxylamineHCID 4691350—
SolventTetrahydrofuranHCID 8028—
Product4-acetyl-N-(tert-butyldimethylsiloxy)benzenesulfonamideHCID 2108252878.9%

Reaction Steps

Ex-33A: To a solution of O-(tert-butyldimethylsilyl)hydroxylamine (0.74 g, 5 mmol) and triethylamine (1.01 g, 10 mmol) in 25 ml THF, 4-acetylbenzenesulfonyl chloride(1.1 g, 5 mmol) was added at 0° C. The mixture was stirred overnight and then poured into H2O. The precipitate was filtered, dried, and recrystallized from EtOAc/Hexene to give 1.3 g (76.8%) of 4-acetyl-N-(tert-butyldimethylsiloxy)benzenesulfonamide as a white solid. 1H-NMR (300 MHz, CDCl3) δ 8.11 (d, J=9 Hz, 2H), 8.01 (d, J=9 Hz, 2H), 6.59 (b, 1H), 2.67 (s, 3H), 0.89 (s, 9H), 0.20 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173129B2
Source datasetuspto-grants-2007_02
ORD IDord-8405d919c0c34009802b017a6c56ebd7
Source noteuspto-grants-2007_02