HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844822Generated: October 31, 2026
Potassium Bicarbonate → HCID 25144318, compound
https://huagongshe.com/reaction/1844822
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 1,3-Dichloro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene | HCID 23159823 | — |
| Reactant | HCID 86070635 | HCID 86070635 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 25144318 | HCID 25144318 | 35.3% |
Reaction Steps
In a solution of 0.45 g of 4-hydroxyiminomethyl-2-methyl-N-(2-pyridylmethyl) benzoic acid amide in 10 ml of N,N-dimethylformamide, 0.25 g of N-chlorosuccinc acid imide was added, and stirred at 70° C. for 1 hour. Then, the reaction mixture was left and cooled to room temperature, 0.41 g of 3,5-dichloro-1-(1-trifluoromethylethenyl)benzene synthesized in Step 1 of Synthetic Example 3 and 0.25 g of potassium hydrogen carbonate were added, and stirred at room temperature for 3 hours. After the completion of the reaction, the reaction mixture was poured in 50 ml of ice water, extracted with ethyl acetate (60 ml×1), the organic phase was dehydrated with saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified with silica gel column chromatography that was eluated with ethyl acetate-hexane (3:1), and 0.30 g of the aimed product was obtained as white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946492B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-e81fb815586f4780ba0b9fe575b29faa |
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| Source note | uspto-grants-2015_02 |
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