HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489370Generated: October 30, 2026
2-Chlorobenzaldehyde → HCID 178439374, compound
https://huagongshe.com/reaction/489370
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | 3-Oxohexanenitrile | HCID 9793723 | — |
| Reactant | HCID 178418806 | HCID 178418806 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178439374 | HCID 178439374 | 36.2% |
Reaction Steps
To a solution of acetonitrile (4.8 g) in THF (150 mL) was added n-BuLi (67 mmol) at −78° C. Further, methyl butanoate (10 g) was added and the mixture was stirred for one hour. After acidification with hydrochloric acid, the mixture was extracted with ethyl acetate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate (10:1)) to give 1-cyanopentan-2-one (5.5 g) as a colorless oil. A solution of 2-chlorobenzaldehyde (1.9 g), 3-aminopyrazole (1.0 g) and 1-cyanopentan-2-one (1.6 g) in acetonitrile (20 mL) was heated under reflux overnight. The reaction mixture was cooled to room temperature, and the precipitated crystals were collected by filtration to give the title compound (1.3 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06977262B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-7ae107ef36c34414a3255deee1d15a25 |
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| Source note | uspto-grants-2005_12 |
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