Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401408Generated: October 25, 2026

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

https://huagongshe.com/reaction/401408

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 numberUS08741925B2
Source datasetuspto-grants-2014_06
ORD IDord-1be328e520154cda92db272a2d22fd2e
Source noteuspto-grants-2014_06