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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83082Generated: October 27, 2026

Trifluoroacetic acid → 1-Benzhydryl-3-(3-methylbenzofuran-2-yl)azetidine

https://huagongshe.com/reaction/83082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBoron trifluoride etherateHCID 8000—
ReactantTriethylsilaneHCID 12052—
Reactant1-Benzhydryl-3-(3-methylbenzofuran-2-yl)azetidin-3-olHCID 67154549—
SolventDichloromethaneHCID 6344—
Product1-Benzhydryl-3-(3-methylbenzofuran-2-yl)azetidineHCID 6715465463%

Reaction Steps

To a cooled (0° C.) solution of 1-benzhydryl-3-(3-methylbenzofuran-2-yl)azetidin-3-ol (406 mg, 1.099 mmol) in dichloromethane (50 mL) were added triethylsilane (1.775 mL, 10.99 mmol) and trifluoroacetic acid (1.630 mL, 22.01 mmol). The reaction mixture was warmed to rt and stirred for 23 h. After 18 h, boron trifluoride etherate (0.6 mL, 4.73 mmol) was added and the reaction was allowed to stir for an additional 5 h. The reaction mixture was partitioned between sat. NaHCO3 and DCM. The layers were separated, the organic layer was washed with sat. NaHCO3 and brine, dried on Na2SO4 and concentrated. The residue was purified by flash chromatography (heptane/EtOAc, 0%→30%), yielding the title product (244 mg, 63%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846711B2
Source datasetuspto-grants-2014_09
ORD IDord-944120d9480b472890df3b5b4b9e85b6
Source noteuspto-grants-2014_09