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HRID 12854作成日:2026年10月26日

Ethyl formate → Ethyl 2-formyl-3-oxopropanoate

https://huagongshe.com/reaction/12854

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl formateHCID 8025—
反応物Ethyl 3,3-diethoxypropionateHCID 66389—
反応物HCID 178418922HCID 178418922—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 2-formyl-3-oxopropanoateHCID 11029955100.1%

反応条件

温度0 °C

反応手順

Ethyl 3,3-diethoxypropionate (100 g, 525.7 mmol) was dissolved in THF (360 ml) at room temp. Ethyl formate (175.1 ml, 2.1 mol) was added at room temp. The solution was cooled in an ice-bath to 0° C. and tBuOK (1M solution in THF, 1,156 ml, 1.156 mol) was added via an addition funnel slowly over 30 min, maintaining internal temperature below 5° C. The color changed instantly from colorless to dark orange. The reaction mixture was allowed to warm up to room temp. and stirred for 2 h. The reaction was allowed to stir at room temp. for 18 h. The reaction mixture was concentrated in vacuo and 1 L of solvent was removed. The remaining brownish solution with white solid in it was cooled in an ice-bath and hydrochloric acid (6N, 200 ml) was added to adjust pH=3, maintaining internal temperature below 20° C. The resulting bright yellow suspension was then warmed up to room temp. and stirred for 1 h. Additional 700 ml solvent was removed in vacuo at room temp. Water (400 ml) was added to dissolve all the white solid and ethyl acetate (500 ml) was added and the mixture transferred to a separatory funnel. The aqueous was extracted once with ethyl acetate (200 ml). The combined organic extracts was washed once with brine (100 ml). After drying over MgSO4 and concentrating in vacuo, 2-formyl-3-oxo-propionic acid ethyl ester (75.85 g) was obtained as yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728029B2
出典データセットuspto-grants-2010_06
ORD IDord-f162d2aee57f4371ba5eb6e5a8135f3d
出典メモuspto-grants-2010_06