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HRID 1242066作成日:2026年10月27日

Ethyl oxoacetate → Ethyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylate

https://huagongshe.com/reaction/1242066

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl oxoacetateHCID 70211—
反応物1-Methoxy-3-trimethylsilyloxy-1,3-butadieneHCID 101051—
触媒ZincchlorideHCID 3007855—
溶媒BenzeneHCID 241—
生成物Ethyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylateHCID 2249509775%

反応手順

A solution of glyoxylic acid ethyl ester, polymer form (2.02 g, 8.9 mmol) and (3-methoxy-1-methylene-allyloxy)-trimethyl-silane (1.9 ml, 8.9 mmol, Danishefsky's diene) in benzene (12 ml) was placed under nitrogen. Zinc chloride (0.5N in tetrahydrofuran, 8.9 ml, 4.45 mmol) was added and the reaction stirred at ambient temperature for 72 h. The mixture was concentrated in vacuo, diluted with ethyl acetate (100 ml) and washed with 1 N hydrochloric acid (20 ml), saturated sodium bicarbonate (20 ml), and brine (20 ml). The organic layer was dried (Na2SO4), filtered, and the solvent evaporated in vacuo. The residue was purified by silica gel chromatography using a mixture of ethyl acetate/hexane (1:2) as eluant. Pure fractions were collected and the solvent evaporated in vacuo which afforded 1.2 g (75%) of 4-oxo-3,4-dihydro-2H-pyran-2-carboxylic acid ethyl ester as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07115624B1
出典データセットuspto-grants-2006_10
ORD IDord-c3730e9cff94473b822c79093dd8dd0b
出典メモuspto-grants-2006_10