HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683147Generated: October 30, 2026
Ethyl benzoylacetate → HCID 11064550, compound
https://huagongshe.com/reaction/1683147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl benzoylacetate | HCID 7170 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 11064550 | HCID 11064550 | 88.5% |
Reaction Steps
In succession at 25° C. and with introduction of nitrogen, 192 g (1 mol) of ethyl benzoyl acetate in 20 min and a solution of 84 g (1.2 mol) of crotonaldehyde in 100 ml of dioxane were added dropwise with stirring in the course of 30 min to a suspension of 2 g of sodium hydride in dioxane. After stirring for 10 hours, the reaction mixture was treated with 800 ml of acetic acid and then with 245 g (3.5 mol) of hydroxylamine hydrochloride. After stirring at 110° C. for 2 hours, the mixture was cooled to 20° C., stirred into 1 kg of ice and rendered alkaline with solid K2CO3. It was then extracted with ethyl acetate, the combined extracts were extracted with 2N HCl solution and the combined aqueous extracts were rendered alkaline with solid K2CO3 and again extracted three times with 300 ml of ethyl acetate each time. After concentrating the combined organic extracts, 62 g of ethyl 2-phenyl-4-methylnicotinate (88.5% of theory) were obtained as a yellowish oil, nD23 =1.5724.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05637554 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-8c2f0dc139384fe18e351e385bd0703f |
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| Source note | uspto-grants-1997_06 |
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