HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244948Generated: October 30, 2026
Trichloroacetyl chloride → HCID 67815290, compound
https://huagongshe.com/reaction/244948
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trichloroacetyl chloride | HCID 6420 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67812414 | HCID 67812414 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67815290 | HCID 67815290 | — |
Reaction Steps
171 mg of 4-(4-hexylphenyl)-5-(methoxymethoxy)-1-(2-methyl-1-(p-tolyl)propan-2-yl)-1H-pyrazole-3-carboxamide was dissolved in 2 mL of methylene chloride and mixed with 0.3 mL (2 mmol) of triethylamine. The reaction solution was cooled to 0° C. in an ice bath, and after dropwise addition of 0.080 mL (0.72 mmol) of trichloroacetyl chloride at room temperature for 1.5 hours. After completion of the reaction, the reaction mixture was mixed with methylene chloride and washed with saturated aqueous sodium hydrogen carbonate and with saturated aqueous sodium chloride successively. The organic layer was dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to give the desired product (crude yield 266 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658686B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-65df71659f8d4cb180f0234434fa2b31 |
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| Source note | uspto-grants-2014_02 |
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