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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111529Generated: November 1, 2026

Tetrahydrofuran → Trifluoroacetic acid

https://huagongshe.com/reaction/2111529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCesium fluorideHCID 25953—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
Reactant1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
ProductTrifluoroacetic acidHCID 6422—
Product1-(Diphenylmethyl)-3-(trifluoromethyl)azetidin-3-olHCID 57639121—

Reaction Steps

To a solution of 1-benzhydryl-azetidin-3-one (400 mg, 1.69 mmol) in THF (5 mL), trifluoromethyltrimethylsilane (360 mg, 2.53 mmol) and cesium fluoride(390 mg, 2.57 mmol) were added. The reaction mixture was stirred at rt. for 1 hr. Then it was quenched with 5 mL saturated NH4Cl solution and tetrabutylammonium fluoride (200 mg) was added. The resulting reaction mixture was stirred at rt. for three days. It was then extracted with ether (3×20 mL). The organic layers were combined, dried (MgSO4) and concentrated to give an orange oil as crude product. It was then purified by Prep.HPLC column to afford a white solid as final product as TFA salt. (350 mg, 49% yield). Retention time: 1.442 min. 1H NMR (500 MHz, MeOD) δ ppm 3.92 (d, J=11.29 Hz, 2 H) 4.35 (d, J=11.60 Hz, 2 H) 5.44 (s, 1 H) 7.34-7.55 (m, 10 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521442B2
Source datasetuspto-grants-2009_04
ORD IDord-95f23482c76e47a4a6fa5bdd54386fba
Source noteuspto-grants-2009_04