Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985131Generated: October 29, 2026

Benzyl Bromide → HCID 68867323, compound

https://huagongshe.com/reaction/1985131

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, 0.172 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 (0.051 g, 0.115 mmol) and sodium hydride (0.011 g, 0.287 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 and concentrated in vacuo to provide the title compound, which is used in 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-0ab18437883a4980a0f0846827e008db
Source noteuspto-grants-2009_06