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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985142Generated: October 28, 2026

Sodium hydride → HCID 10289584, compound

https://huagongshe.com/reaction/1985142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
ReactantHCID 68867329HCID 68867329—
CatalystTetrabutylammonium IodideHCID 67553—
SolventEthyl AcetateHCID 8857—
ProductHCID 10289584HCID 10289584—

Reaction Steps

4-Chlorobenzyl bromide (0.035 g, 0.172 mmol) 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. The organic layer is dried, concentrated, and purified by LCMS to provide the title compound. 1H NMR (400 MHz, CDCl3): δ 7.31-7.22 (m, 5H), 7.15-7.01 (m, 5H), 6.74 (d, 2H, J=7.8 Hz), 4.34 (d, 2H, J=14.3 Hz), 3.96 (s, 2H), 3.73-3.71 (m, 1H), 3.46-3.40 (m, 1H), 3.28, 3.16 (ABq, 2H, J=14.3 Hz), 3.08-3.06 (m, 1H), 2.85 (s, 3H), 2.23-2.20 (m, 1H), 1.91-1.89 (m, 1H), 1.41 (s, 3H). MS [ES+] m/z exact mass calcd for C29H31N2O5FCl 541.1906, found 541.1909.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544812B2
Source datasetuspto-grants-2009_06
ORD IDord-a76e719b0dc04e30a6e9cddee9cc0c5a
Source noteuspto-grants-2009_06