HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878065Generated: October 31, 2026
Phenylacetyl chloride → HCID 67050467, compound
https://huagongshe.com/reaction/1878065
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Aminopyridine-2-carbonitrile | HCID 3871395 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67050467 | HCID 67050467 | — |
Reaction Steps
To a suspension of 5-amino-2-cyanopyridine (0.500 g, 4.2 mmol) in dry dichloromethane (20 mL) was added triethylamine (0.637 g, 6.3 mmol) and the mixture was stirred at 0° C. To the reaction mixture phenylacetyl chloride (0.973 g, 6.3 mmol) was added dropwise and stirred at 0° C. for 1 hour and then at room temperature for 24 hours. The reaction mixture was diluted with chloroform (100 mL) and washed with water (150 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated to obtain the crude product, which was purified using column chromatography (silica gel, 20% ethyl acetate in petroleum ether as an eluent) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314103B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-073de9e717b644f197515fc98da01cb0 |
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| Source note | uspto-grants-2012_11 |
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