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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477587Generated: October 29, 2026

Tetrahydrofuran → HCID 117849124, compound

https://huagongshe.com/reaction/1477587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant4-Fluorobenzyl bromideHCID 68021—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 117849124HCID 11784912449%

Reaction Steps

To a tetrahydrofuran solution (2.0 mL) of tert-butyl 3-hydroxyazetidine-1-carboxylate (87 mg, 0.50 mmol), sodium hydride (33 mg, 0.75 mmol, purity 55%) was added at 0° C. and the resultant solution was stirred for 30 minutes. Subsequently, 4-fluorobenzyl bromide (62.3 μL, 0.50 mmol) was added to the reaction solution and the resultant mixture was stirred at room temperature for 19 hours. After completion of the reaction, water was added to the reaction solution and extraction with ethyl acetate from the resultant mixture was performed three times. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (68.5 mg, yield 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-1a62f771c35346cb96d41f904f94339a
Source noteuspto-grants-2016_08