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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800634Generated: October 31, 2026

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

https://huagongshe.com/reaction/1800634

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 under a hydrogen atmosphere (1 atm) at room temperature 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 numberUS08344135B2
Source datasetuspto-grants-2013_01
ORD IDord-80fa19a70fc049a88c6bf7cd288b025e
Source noteuspto-grants-2013_01