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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711289Generated: October 30, 2026

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

https://huagongshe.com/reaction/1711289

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Nitro-phenyl)-ethanesulfonic acid tert-butylamideHCID 68505559—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(4-Amino-phenyl)-ethanesulfonic acid tert-butylamideHCID 6850490195%

Reaction Steps

2-(4-Nitro-phenyl)-ethanesulfonic acid tert-butylamide (as prepared in the step above, 633 mg, 2.21 mmol) was hydrogenated under balloon pressure in EtOH (20 mL) using 10% Pd/C (100 mg) for 12 h. The reaction mixture was filtered through Celite and concentrated to obtain 2-(4-amino-phenyl)-ethanesulfonic acid tert-butylamide (536 mg, 95%) which was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790724B2
Source datasetuspto-grants-2010_09
ORD IDord-5077d8a82268484e893dd356757dc5c4
Source noteuspto-grants-2010_09