HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467863Generated: October 30, 2026
HCID 2778795, compound → HCID 178474418, compound
https://huagongshe.com/reaction/467863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 2778795 | HCID 2778795 | — |
| Reactant | HCID 178475102 | HCID 178475102 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178474418 | HCID 178474418 | 25.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08623880B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-99077d4200674b38a3e8873636f0402c |
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| Source note | uspto-grants-2014_01 |
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