HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366339Generated: October 30, 2026
Dimethylformamide → HCID 23289161, compound
https://huagongshe.com/reaction/366339
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23289174 | HCID 23289174 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23289161 | HCID 23289161 | 74.3% |
Reaction Steps
20 ml of N,N-dimethylformamide was added to 0.8 g (1.6 mmol) of 3-[4-chloro-2-(1-chloroethyl)-3-ethoxycarbonyl-6-fluorobenzofuran-7-yl]-1-methyl-6-trifluoromethyluracil, 0.16 g (2.5 mmol) of potassium cyanide and 0.40 g (2.9 mmol) of potassium carbonate, followed by stirring at room temperature for 3 hours. After completion of the reaction, the reaction solution was poured into water and extracted with ethyl acetate. The organic layer was washed sequentially with water and a saturated sodium chloride aqueous solution and then, dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. Then, the obtained residue was purified by silica gel column chromatography to obtain 0.58 g (yield: 74%) of the desired product as a yellow glassy substance. Refractive index: 1.5348 (20° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06130187 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-6623c4fbcd2b44718b650016086afa03 |
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| Source note | uspto-grants-2000_10 |
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