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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570811Generated: October 25, 2026

Potassium Carbonate → 3-(2-Chloro-4-fluorophenoxy)-1-(diphenylmethyl)azetidine

https://huagongshe.com/reaction/570811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-fluorophenolHCID 74814—
Reactant1-(Diphenylmethyl)azetidin-3-yl methanesulfonateHCID 2758716—
SolventAcetonitrileHCID 6342—
Product3-(2-Chloro-4-fluorophenoxy)-1-(diphenylmethyl)azetidineHCID 15042226—

Reaction Steps

A mixture of 1-(diphenylmethyl)-3-azetidinyl methanesulfonate (363.8 g, 1.15 mol), potassium carbonate (330 g, 2.38 mol) and 2-chloro-4-fluorophenol (140 g, 0.96 mol) in acetonitrile (2.5 L) was heated under reflux for 4.5 hours. The cooled reaction mixture was then concentrated in vacuo and the residue was partitioned between ethyl acetate (1 L) and water (500 mL). The organic layer was separated, dried over sodium sulfate concentrated in vacuo and the residue was triturated with ethyl acetate/pentane/dichloromethane, 90:10:1, to afford the title compound as a white solid in quantitative yield, 350 g. 1H NMR (400 MHz, CDCl3) δ: 3.19 (m, 2H), 3.75 (m, 2H), 4.45 (m, 1H), 4.78 (m, 1H), 6.60 (m, 1H), 6.83 (m, 1H), 7.14 (m, 1H), 7.18-7.50 (m, 10H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023872B2
Source datasetuspto-grants-2015_05
ORD IDord-ff77a4901a444d52a9be963bbf0d647b
Source noteuspto-grants-2015_05