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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401341Generated: October 26, 2026

Ammonium formate → 1-Tert-butyl-2-methoxy-5-(trifluoromethyl)-4-aminobenzene

https://huagongshe.com/reaction/401341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-Tert-butyl-2-methoxy-5-(trifluoromethyl)-4-nitrobenzeneHCID 57470246—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-Tert-butyl-2-methoxy-5-(trifluoromethyl)-4-aminobenzeneHCID 5747024795.9%

Reaction Steps

To a refluxing solution of 1-tert-butyl-2-methoxy-5-(trifluoromethyl)-4-nitrobenzene (473 mg, 1.7 mmol) and ammonium formate (473 mg, 7.3 mmol) in EtOH (10 mL) was added 10% Pd—C (200 mg). The mixture was refluxed for 1 h, cooled and filtered through Celite. The solvent was removed by evaporation to give 1-tert-butyl-2-methoxy-5-(trifluoromethyl)-4-aminobenzene (C-18) (403 mg, 95%). 1H NMR (400 MHz, CDCl3) δ 7.19 (s, 1H), 6.14 (s, 1H), 4.02 (bs, 2H), 3.74 (s, 3H), 1.24 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741925B2
Source datasetuspto-grants-2014_06
ORD IDord-5f3259e30dd247e883b03d1a8698f2e4
Source noteuspto-grants-2014_06