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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041887Generated: November 1, 2026

Water → 3-(3-Chloro-5-fluorophenyl)-1-ethylazetidin-3-ol

https://huagongshe.com/reaction/2041887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(3-Chloro-5-fluorophenyl)azetidin-3-olHCID 66995393—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product3-(3-Chloro-5-fluorophenyl)-1-ethylazetidin-3-olHCID 4620810760.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3-(3-chloro-5-fluorophenyl)azetidin-3-ol (0.41 g, 2.03 mmol), potassium carbonate (0.56 g, 4.06 mmol) and iodoethane (0.31 g, 2.03 mmol) in acetonitrile (5 ml) was heated at 120° C. under microwave irradiation for 10 min. Water (50 ml) and ethyl acetate (50 ml) was added and the organic phase was collected. The aqueous phase was extracted with ethyl acetate (2×50 ml). The combined organic phase was dried (Na2SO4) and evaporated under reduced pressure to give the crude product. Purification by flash column chromatography on silica gel (ethyl acetate) gave 0.28 g (60%) of the title compound. The amine was converted to the fumaric acid salt and recrystallized from ethanol/diethyl ether/diisopropyl ether: M.p. 166-168° C. MS m/z (relative intensity, 70 eV) 229 (M+, 1), 172 (23), 130 (24), 109 (33), 58 (bp).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586572B2
Source datasetuspto-grants-2013_11
ORD IDord-4652aae95b8240f3b3f5d251a489b02e
Source noteuspto-grants-2013_11