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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536040Generated: October 30, 2026

Isopropanol → 4-Isopropoxy-N-methyl-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/536040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant4-fluoro-N-methyl-3-nitrobenzenesulfonamideHCID 8468085—
SolventWaterHCID 962—
Product4-Isopropoxy-N-methyl-3-nitrobenzenesulfonamideHCID 6993523858%

Reaction Steps

NaH (0.440 g, 11 mmol) was added to 20 mL of isopropanol and the resulting mixture stirred at room temperature. After 30 minutes, 4-fluoro-N-methyl-3-nitrobenzenesulfonamide (2.34 g, 10 mmol) was added. The reaction mixture was then stirred at room temperature overnight. The mixture was poured into EtOAc and water. The organic phase was separated, dried over Na2SO4, and concentrated in vacuo to give the crude product. Purification via column chromatography (1:1 petroleum ether/ethyl acetate) afforded N-methyl-4-[(1-methylethyl)oxy]-3-nitrobenzenesulfonamide (1.6 g, 58% yield) as a yellow solid. MS (m/z) 274.7 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859571B2
Source datasetuspto-grants-2014_10
ORD IDord-16445e4b802040e1b77f22b45efca9d6
Source noteuspto-grants-2014_10