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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12400Generated: October 26, 2026

4-Fluorophenol → (2-(4-Fluorophenoxy)-ethyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/12400

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
SolventDimethylformamideHCID 6228—
Product(2-(4-Fluorophenoxy)-ethyl)-carbamic acid tert-butyl esterHCID 23134036—

Reaction Conditions

Temperature90 °C

Reaction Steps

To the crude product (700 mg) of t-butyl 2-bromoethylcarbamate obtained in Step 1 were added 4-fluorophenol (875 mg), potassium carbonate (1.08 g) and DMF (7 ml), and the mixture was stirred overnight at 90° C. The solvent was evaporated, and the mixture was diluted with ethyl acetate. After washing with water, the organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated. The obtained crude product was purified by silica gel chromatography (ethyl acetate-hexane) to give t-butyl 2-(4-fluorophenoxy)ethylcarbamate (390 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728005B2
Source datasetuspto-grants-2010_06
ORD IDord-1f2d8b6dfd7647258a6c9672414d151f
Source noteuspto-grants-2010_06