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HRID 233585作成日:2026年10月26日

Water → Ethyl acetylphenylacetate

https://huagongshe.com/reaction/233585

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl phenylacetateHCID 7590—
反応物Ethyl AcetateHCID 8857—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl acetylphenylacetateHCID 9538952.5%

反応条件

温度-78 °C

反応手順

A stirred solution of 10 grams (0.061 mole) of ethyl phenylacetate in 125 mL of tetrahydrofuran is cooled to -78° C., and 33.5 mL (0.067 mole) of lithium diisopropylamide (2M solution in heptane-tetrahydrofuranethylbenzene) is slowly added dropwise at a rate to maintain the reaction mixture temperature below -60° C. Upon completion of addition, the reaction mixture is stirred at -78° C. for about one hour. After this time, 6.5 mL (0.067 mole) of ethyl acetate is added dropwise. Upon completion of addition, the reaction mixture is stirred for about one hour at -78° C. The reaction mixture is then allowed to warm to ambient temperature. After this time the reaction mixture is poured into 200 mL of water, and the mixture is extracted with one 100 mL portion of diethyl ether. The aqueous layer is made acidic with aqueous 10% hydrochloric acid, and then it is extracted with three 150 mL portions of diethyl ether. The combined extracts are dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure, yielding 6.6 grams of ethyl 3-oxo-2-phenylbutanoate. The NMR spectrum is consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05593998
出典データセットuspto-grants-1997_01
ORD IDord-0ccf10fcee0f424c992748878ade357d
出典メモuspto-grants-1997_01