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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189691Generated: October 31, 2026

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

https://huagongshe.com/reaction/2189691

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 numberUS08324242B2
Source datasetuspto-grants-2012_12
ORD IDord-79c937a1bcb74ed9b431aa6486827afb
Source noteuspto-grants-2012_12