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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915404Generated: October 30, 2026

Ammonium Hydroxide → 2-Tert-butyl-5-nitrobenzene-1-sulfonamide

https://huagongshe.com/reaction/1915404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Tert-butyl-5-nitrobenzene-1-sulfonyl chlorideHCID 57470264—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-Tert-butyl-5-nitrobenzene-1-sulfonamideHCID 5747026534%

Reaction Steps

To a solution of 2-tert-butyl-5-nitrobenzene-1-sulfonyl chloride (100 mg, 0.36 mmol) in ether (2 mL) was added aqueous NH4OH (128 μL, 3.6 mmol) at 0° C. The mixture was stirred at room temperature overnight, diluted with water and extracted with ether. The combined ether extracts were washed with brine and dried over Na2SO4. After removal of solvent, the residue was purified by column chromatography (0-50% EtOAc-Hexane) to give 2-tert-butyl-5-nitrobenzene-1-sulfonamide (31.6 mg, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614327B2
Source datasetuspto-grants-2013_12
ORD IDord-a2edd597d0f149c29be6bb5d90c3d7ee
Source noteuspto-grants-2013_12