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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683147Generated: October 30, 2026

Ethyl benzoylacetate → HCID 11064550, compound

https://huagongshe.com/reaction/1683147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl benzoylacetateHCID 7170—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium hydrideHCID 24758—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantCrotonaldehydeHCID 447466—
SolventAcetic AcidHCID 176—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 11064550HCID 1106455088.5%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637554
Source datasetuspto-grants-1997_06
ORD IDord-8c2f0dc139384fe18e351e385bd0703f
Source noteuspto-grants-1997_06