HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860415Generated: October 30, 2026
Pyridine → Ethyl 7-acetyl-7-(4-cyanobenzoyl)-8-oxononanoate
https://huagongshe.com/reaction/860415
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Cyanobenzoyl chloride | HCID 80172 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Reactant | Ethyl 7-acetyl-8-oxononanoate | HCID 14691968 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 7-acetyl-7-(4-cyanobenzoyl)-8-oxononanoate | HCID 57444529 | 57.4% |
Reaction Steps
To a mixture of ethyl 7-acetyl-8-oxononanoate (4.0 g) and magnesium chloride (1.27 g) in dichloromethane (70 ml) was added pyridine (2.15 ml) at 0° C. The mixture was stirred at 20° C. for 1 hour, then a solution of 4-cyanobenzoyl chloride (2.87 g) in dichloromethane (10 ml) was added. After stirring for 3 hours at 20° C., the mixture was partitioned between ether and 1N hydrochloric acid. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:5) to give ethyl 7-acetyl-7-(4-cyanobenzoyl)-8-oxononanoate (3.52 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153854B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-9f60228310a348638454aac9d84d4d3c |
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| Source note | uspto-grants-2006_12 |
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