Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264615Generated: November 1, 2026

Bromide ion → HCID 18612902, compound

https://huagongshe.com/reaction/1264615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantSodium hydrideHCID 24758—
Reactant2-(Bromomethyl)-4-fluoro-1-nitrobenzeneHCID 10561643—
ReactantN-[[4-(2-Butyn-1-yloxy)phenyl]sulfonyl]serine methyl esterHCID 12016494—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 18612902HCID 1861290284.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution was of 2-(bromomethyl)-4-fluoro-1-nitrobenzene (1.3 g, 5.56 mmol) at 0° C. was added tetrabutylammonium iodide (2.05 g, 5.56 mmol). The solution was stirred at 0° C. for 1.5 hours. In a separate flask, methyl 2-({[4-(2-butynyloxy)phenyl]sulfonyl}amino)-3-hydroxypropanoate (1.73 g, 5.05 mmol) was dissolved in dimethylformamide and cooled to 0° C. Sodium hydride (0.21 g, 5.56 mmol, 60% dispersion in oil) was added and the reaction was allowed to stir at 0° C. for 0.5 hours at which time the solution of the bromide was added. The reaction was stirred overnight and then quenched with water. The mixture was extracted twice with ethyl acetate, washed with brine, dried over Na2SO4, concentrated in vacuo and chromatographed using 1.5:1 hexane:ethyl acetate as eluant to provide 1.88 g (77%) of the desired product as a white solid. mp 83-88° C. Anal Calc'd for C21H21N2O8FS: C, 52.50; H, 4.41; N, 5.83. Found: C, 52.44; H, 4.76; N, 5.56.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544984B1
Source datasetuspto-grants-2003_04
ORD IDord-aa94157ae0814b4e88941edb88c54668
Source noteuspto-grants-2003_04