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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184897Generated: October 27, 2026

Water → N-tert-butyl-4'-aminobiphenyl-2-sulfonamide

https://huagongshe.com/reaction/2184897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-BromoanilineHCID 7807—
ReactantSodium HydroxideHCID 14798—
ReactantBoronic acid, B-(2-(((1,1-dimethylethyl)amino)sulfonyl)phenyl)-HCID 4997616—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventIsopropanolHCID 3776—
ProductN-tert-butyl-4'-aminobiphenyl-2-sulfonamideHCID 10804475—

Reaction Steps

To a solution of 2-[(tert-butyl amino)sulfonyl]phenyl boronic acid (6.00 g, 23.35 mmol) in 120 ml toluene was added water (16 ml), isopropanol (60 ml), and NaOH (40 ml, 5M aqueous solution). To this were added 4-bromoaniline and Pd(Ph3P)4. This heterogeneous mixture is then refluxed for 6 hr, then stirred at room temperature over night before refluxing for another 1.5 hr. The reaction mixture is then extracted with water and ethyl acetate. The aqueous layer is extracted twice with ethyl acetate. The organic layers are then dried over MgSO4, filtered and concentrated in vacuo. The crude residue is purified by silica gel flash chromatography. The desired product can be eluded with 30% ethyl acetate in hexanes and concentrated to an orange solid (5.06 g, 16.65, 71%). ES-MS(M+H)+=305.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399627B1
Source datasetuspto-grants-2002_06
ORD IDord-bcccea36aa9742b2b3de1585fd020e06
Source noteuspto-grants-2002_06