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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467863Generated: October 30, 2026

HCID 2778795, compound → HCID 178474418, compound

https://huagongshe.com/reaction/467863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 2778795HCID 2778795—
ReactantHCID 178475102HCID 178475102—
SolventAcetonitrileHCID 6342—
ProductHCID 178474418HCID 17847441825.5%

Reaction Steps

To a stirred solution of 2-bromo-1-[3-fluoro-4-(trifluoromethyl)phenyl]ethanone (4.5 g, 15.73 mmol) in acetonitrile (45 ml) was added acetyl guanidine (2.38 g, 23.60 mmol). The reaction mixture was stirred and refluxed for overnight. The solvent was evaporation under reduced pressure and diluted with water and extracted with ethyl acetate (75 ml×3) and organic layers were washed with brine, dried (Na2SO4) and filtered. The filtrate was concentrated under reduced pressure and the residue obtained after the evaporation of the solvent was purified by silica gel column chromatography using 2% methanol in chloroform to obtain 1.15 g of the product as a yellow solid; 1H NMR (300 MHz, DMSO-d6): δ 2.07 (s, 3H), 7.58 (s, 1H), 7.69-7.78 (m, 3H), 11.31 (br s, 1H), 11.91 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623880B2
Source datasetuspto-grants-2014_01
ORD IDord-99077d4200674b38a3e8873636f0402c
Source noteuspto-grants-2014_01