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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711288Generated: November 1, 2026

Tert-Butylamine → 2-(4-Nitro-phenyl)-ethanesulfonic acid tert-butylamide

https://huagongshe.com/reaction/1711288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
Reactant2-(4-nitrophenyl)ethanesulfonyl ChlorideHCID 2761175—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Nitro-phenyl)-ethanesulfonic acid tert-butylamideHCID 6850555962%

Reaction Steps

To a solution of tert-BuNH2 (15.6 mL, 148 mmol) in THF (50 mL) at 0° C., 2-(4-nitro-phenyl)-ethanesulfonyl chloride (WO 2006010079, 1.9 g, 7.6 mmol) was added portionwise. The resulting mixture was stirred for 24 h at RT. The solvent was removed in vacuo and the residue was taken up in DCM (50 mL) and cold 0.5 N HCl (50 mL). The organic layer was separated, dried (Na2SO4) and concentrated to obtain 2-(4-nitro-phenyl)-ethanesulfonic acid tert-butylamide (1.3 g, 62%) which was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790724B2
Source datasetuspto-grants-2010_09
ORD IDord-104fb777ceed4c918a161632e419da38
Source noteuspto-grants-2010_09