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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377171Generated: November 2, 2026

Benzyl Bromide → HCID 21990155, compound

https://huagongshe.com/reaction/2377171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant1-(3-(2-(1-Benzothiophen-5-yl)ethoxy)propionyl)azetidin-3-olHCID 21990049—
CatalystHCID 178418778HCID 178418778—
SolventDimethylformamideHCID 6228—
ProductHCID 21990155HCID 21990155—

Reaction Steps

In 8 mL of N,N-dimethylformamide was dissolved 1.00 g of 3-[2-(1-benzothiophen-5-yl)ethoxy]-1-(3-hydroxy-1-azetidinyl)-1-propanone, and 1.90 g of silver(I) oxide and 0.97 mL of benzyl bromide were added to the solution, after which the resulting mixture was stirred at room temperature for 31 hours. The insoluble materials were filtered off and water and ethyl acetate were added to the residue, after which the organic layer was separated. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; toluene:ethyl acetate=3:1 to 1:4) to obtain 1.00 g of 3-[2-(1-benzothiophen-5-yl)ethoxy]-1-[3-(benzyloxy)-1-azetidinyl]-1-propanone as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468443B2
Source datasetuspto-grants-2008_12
ORD IDord-970706b6409e420b8b6b9eaf511b0c24
Source noteuspto-grants-2008_12