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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477588Generated: October 30, 2026

Dimethylformamide → tert-Butyl 3-(4-fluorophenoxy)azetidine-1-carboxylate

https://huagongshe.com/reaction/1477588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-FluorophenolHCID 9732—
ReactantCesium carbonateHCID 10796—
Reactanttert-Butyl 3-(tosyloxy)azetidine-1-carboxylateHCID 57351432—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 3-(4-fluorophenoxy)azetidine-1-carboxylateHCID 10190906873%

Reaction Steps

An N,N-dimethylformamide solution (1.5 mL) of tert-butyl 3-(tosyloxy)azetidine-1-carboxylate (164 mg, 0.50 mmol), 4-fluorophenol (67.3 mg, 0.60 mmol), and cesium carbonate (116 mg, 0.60 mmol) was stirred at 80° C. for 16 hours. After completion of the reaction, water was added to the reaction solution and extraction with ethyl acetate from the resultant mixture was performed three times. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (97.4 mg, yield 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-d413849aaeb94910b46c2aea2b4da8fb
Source noteuspto-grants-2016_08