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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423809Generated: October 29, 2026

Ammonium formate → 2-Tert-butyl-4-fluoro-6-aminophenyl methyl carbonate

https://huagongshe.com/reaction/423809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant2-Tert-butyl-4-fluoro-6-nitrophenyl methyl carbonateHCID 57470217—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-Tert-butyl-4-fluoro-6-aminophenyl methyl carbonateHCID 5747022627%

Reaction Steps

To a refluxing solution of 2-tert-butyl-4-fluoro-6-nitrophenyl methyl carbonate (250 mg, 0.92 mmol) and ammonium formate (250 mg, 4 mmol) in EtOH (10 mL) was added 5% Pd—C (170 mg). The mixture was refluxed for additional 1 h, cooled and filtered through Celite. The solvent was removed by evaporation and the residue was purified by column chromatography (0-15%, EtOAc-Hexane) to give 2-tert-butyl-4-fluoro-6-aminophenyl methyl carbonate (C-6) (60 mg, 27%). HPLC ret. time 3.35 min, 10-99% CH3CN, 5 min run; ESI-MS 242.0 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101767B2
Source datasetuspto-grants-2012_01
ORD IDord-c1f4590321fb476d9c7311525f96e1b2
Source noteuspto-grants-2012_01