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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985140Generated: October 29, 2026

Benzyl Bromide → HCID 68867323, compound

https://huagongshe.com/reaction/1985140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 68867329HCID 68867329—
CatalystTetrabutylammonium IodideHCID 67553—
SolventEthyl AcetateHCID 8857—
ProductHCID 68867323HCID 68867323—

Reaction Steps

Benzyl bromide (0.02 mL, 0.179 mmol, d=1.438) and tetrabutyl ammonium iodide (catalytic amount) are added to a 0° C. suspension of 2-(2-Fluoro-phenoxy)-2-methyl-3-{4-[2-(3-methyl-2-oxo-imidazolidin-4-yl)-ethoxy]-phenyl}-propionic acid ethyl ester (0.053 g, 0.119 mmol) and sodium hydride (0.012 g, 0.298 mmol, 60% suspension on mineral oil), pre-stirred for 1 h at ambient temperature. The reaction mixture is stirred at ambient temperature for 18 h, diluted with ethyl acetate, and washed with 1N HCl, water, and brine. The organic layer is dried over MgSO4 and concentrated in vacuo to provide the title compound, which is carried into the next step. MS [EI+] 535 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544812B2
Source datasetuspto-grants-2009_06
ORD IDord-b03bcbc6012547a7926b4fb38ef7fb25
Source noteuspto-grants-2009_06