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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78322Generated: October 26, 2026

4-(3-(N-methylsulfamoyl)phenyloxy)benzene → 4-(3-(N-methylsulfamoyl)phenyloxy)-1-nitrobenzene

https://huagongshe.com/reaction/78322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-(N-methylsulfamoyl)phenyloxy)benzeneHCID 23614573—
ReactantSodium NitriteHCID 23668193—
SolventTrifluoroacetic acidHCID 6422—
Product4-(3-(N-methylsulfamoyl)phenyloxy)-1-nitrobenzeneHCID 2361457256.9%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 4-(3-(N-methylsulfamoyl)phenyloxy)benzene (0.30 g, 1.14 mmol) in TFA (6 mL) at −10° C. was added NaNO2 (0.097 g, 1.14 mmol) in portions over 5 min. The resulting solution was stirred at −10° C. for 1 h, then was allowed to warm to room temp., and was concentrated under reduced pressure. The residue was separated between EtOAc (10 mL) and water (10 mL). The organic phase was sequentially washed with water (10 mL) and a saturated NaCl solution (10 mL), dried (MgSO4) and concentrated under reduced pressure to give 4-(3-(N-methylsulfamoyl)phenyloxy)-1-nitrobenzene (0.20 g). This material carried on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841330B2
Source datasetuspto-grants-2014_09
ORD IDord-fec1a8ae21b34a8190d0d736409d9dab
Source noteuspto-grants-2014_09