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HRID 21355作成日:2026年10月26日

Ethyl Acetoacetate → 2-(2-Ethoxycarbonyl-3-oxobutyl)naphthalene

https://huagongshe.com/reaction/21355

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetoacetateHCID 8868—
反応物2-BromomethylnaphthaleneHCID 70320—
反応物SodiumHCID 5360545—
溶媒EthanolHCID 702—
生成物2-(2-Ethoxycarbonyl-3-oxobutyl)naphthaleneHCID 13926107114.1%

反応手順

In a four-necked flask equipped with a thermometer, dropping funnel and stirrer were placed 179 g (1.375 moles) of ethyl acetoacetate and 500 ml of ethanol, and then 31.5 g (1.375 moles) of sodium was added in portions thereto to form a solution. Then, a solution of 276.4 g (1.25 moles) of 2-bromomethylnaphthalene in 1000 ml of ethanol was added dropwise to the above solution at room temperature over a period of 2 hours. After completion of the addition, the resulting mixture was brought up to 65° C. and stirred at the same temperature for 6 hours. After completion of the reaction ethanol was distilled off under reduced pressure, the residue obtained was extracted by addition of 1500 ml of toluene, and the organic layer was separated. The organic layer was washed with 10% hydrochloric acid, water, 5% aqueous sodium bicarbonate solution and water in said order and then concentrated under reduced pressure to obtain 385.4 g of 2-(2-ethoxycarbonyl-3-oxobutyl)naphthalene as a crude product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05422038
出典データセットuspto-grants-1995_06
ORD IDord-66573b26e9d24df49d64b3e512da4a5e
出典メモuspto-grants-1995_06