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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602671Generated: October 30, 2026

P-Chloroacetophenone → Methyl {1-[1-(4-chlorophenyl)ethyl]azetidin-3-ylidene}(3,5-difluorophenyl)acetate

https://huagongshe.com/reaction/602671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ChloroacetophenoneHCID 7467—
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl azetidin-3-ylidene(3,5-difluorophenyl)acetateHCID 67065925—
Solvent1,1-DichloroethaneHCID 6365—
ProductMethyl {1-[1-(4-chlorophenyl)ethyl]azetidin-3-ylidene}(3,5-difluorophenyl)acetateHCID 67065932—

Reaction Steps

A solution of 0.142 g (0.5 mmole) of methyl azetidin-3-ylidene(3,5-difluorophenyl)acetate, 0.142 g (1 mmol) of 4-chloroacetophenone and 0.15 mL (12 mmol) of triethylamine in 5 mL of dichloroethane was stirred at room temperature. After 5 min, 0.422 g (2 mmol) of sodium triacetoxyborohydride was added and the mixture was stirred at room temperature for 3 h. The reaction was quenched by addition of saturated KHCO3 solution and the mixture was partitioned between 10 mL ether and 2 mL saturated KHCO3 solution. The layers were separated and the organic layer was dried over Na2SO4, and concentrated. The residue was purified by reverse phase chromatography (Waters Xterra C18, 19 mm×10 mm) using a gradient of CH3CN—H2O-Et3N (20:80:0.1 to 60:40:0.1) to afford the title compound; Mass Spectrum: m/e=378 (M+1 35Cl) and 380 (M+1 35Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906503B2
Source datasetuspto-grants-2011_03
ORD IDord-0de440b1db484c91a738633f6dce88c8
Source noteuspto-grants-2011_03