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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48346Generated: October 26, 2026

1-(5-Amino-2-fluorophenyl)ethanone → tert-butyl N-(3-acetyl-4-fluorophenyl)carbamate

https://huagongshe.com/reaction/48346

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Amino-2-fluorophenyl)ethanoneHCID 2781125—
ReactantTert-butyldicarbonateHCID 22064466—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl N-(3-acetyl-4-fluorophenyl)carbamateHCID 6989215373.7%

Reaction Steps

To a solution of 1.19 g (7.77 mmol) of 1-(5-amino-2-fluorophenyl)ethanone in 18 ml of dry tetrahydrofuran at room temperature under an atmosphere of nitrogen was added 1.86 g (8.54 mol) of tert-butyl dicarbonate. The solution was stirred for 28 hours at room temperature followed by 17 hours at 45° C., cooled to room temperature and evaporated under reduced pressure. The residue was dissolved in ethyl acetate and the solution washed with sodium bicarbonate solution, dried over magnesium sulphate, evaporated to dryness and the residue chromatographed on silica gel using ethyl acetate/petrol 4:1 for the elution. There was obtained 1.45 g of (3-acetyl-4-fluorophenyl)carbamic acid tert-butyl ester MS: m/e 271 [M+CH3CN]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703387B2
Source datasetuspto-grants-2004_03
ORD IDord-eb4b1ec7feed439285bc1d43c0f88051
Source noteuspto-grants-2004_03