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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292736Generated: October 29, 2026

Dichloromethane → 1-benzhydryl-3-fluoroazetidine

https://huagongshe.com/reaction/1292736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-(Diphenylmethyl)azetidin-3-olHCID 330448—
ReactantSodium BicarbonateHCID 516892—
Reactant(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
SolventWaterHCID 962—
Product1-benzhydryl-3-fluoroazetidineHCID 7330507—

Reaction Steps

A 250 mL, round bottom flask was charged with 3.0 g (12.5 mmol) of 1-benzhydryl-3-hydroxyazetidine and 80 mL of dichloromethane. To the stirring solution at −78° C. was added 4.6 mL (25 mmol) of [bis(2-methoxyethyl)amino]sulfur trifluoride via addition funnel over a period of about 3 h. The reaction mixture was allowed to warm slowly to ambient temperature overnight. The reaction mixture was added portionwise (with caution) to a large extractor containing water and saturated aqueous sodium bicarbonate solution. The mixture was extracted three times with 80 mL of dichloromethane. The combined organic layers were washed sequentially with saturated aqueous sodium bicarbonate solution, water and saturated aqueous brine, dried over sodium sulfate, and concentrated in vacuo. Purification by flash chromatography using a Biotage® system (gradient, hexane to 80% ethyl acetate/hexane) afforded the desired product. LC/MS 242.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238683B2
Source datasetuspto-grants-2007_07
ORD IDord-eead71c4ac2d47849e6a2237e198bcb3
Source noteuspto-grants-2007_07