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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366748Generated: October 31, 2026

tert-Butyl [(4-fluoro-3-nitrophenyl)methyl]carbamate → tert-Butyl [(3-amino-4-fluorophenyl)methyl]carbamate

https://huagongshe.com/reaction/2366748

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl [(4-fluoro-3-nitrophenyl)methyl]carbamateHCID 53420783—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Producttert-Butyl [(3-amino-4-fluorophenyl)methyl]carbamateHCID 5343922299%

Reaction Steps

To a solution of tert-butyl (4-fluoro-3-nitrophenyl)methylcarbamate (1.0 g, 3.70 mmol) in methanol (4 mL) was added 10% palladium-carbon (150 mg), and the mixture was stirred at room temperature under a hydrogen atmosphere (1 atm) for 18 hr. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate), and the obtained solution was concentrated under reduced pressure to give the title compound (0.88 g, 99%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697874B2
Source datasetuspto-grants-2014_04
ORD IDord-fbd03f4d51af4a36990ed0dbf1abd520
Source noteuspto-grants-2014_04