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HRID 220489作成日:2026年10月25日

Ethyl bromoacetate → Ethyl 4-oxo-3-propanoylhexanoate

https://huagongshe.com/reaction/220489

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物Sodium hydrideHCID 24758—
反応物3,5-HeptanedioneHCID 81923—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 4-oxo-3-propanoylhexanoateHCID 5098800477%

反応条件

温度0 °C

反応手順

Dissolve heptane-3,5-dione (2.5 g, 19.5 mmol) in dry tetrahydrofuran (10 mL) and add the resulting solution dropwise to a chilled (0° C.) suspension of sodium hydride (0.94 g, 23.4 mmol, 60% dispersion in oil) in tetrahydrofuran (20 mL). Stir at 0° C. for 1 hr., then add bromoacetic acid ethyl ester (2.6 mL, 23.4 mmol) dropwise. Stir for 16 hr. at 0° C. and warm to room temperature. Partition the reaction mixture between diethyl ether (100 mL) and saturated aqueous ammonium chloride solution (50 mL). Separate the organic layer and wash with saturated aqueous sodium chloride solution (50 mL), dry (sodium sulfate), filter and concentrate. Purify using silica gel chromatography, eluting with 10:1 hexanes:ethyl acetate, to give 4-oxo-3-propionyl-hexanoic acid ethyl ester as an oil (3.2 g, 77%). 1H-NMR (400 MHz, CDCl3) δ 4.08 (m, 3H), 2.83 (d, 2H), 2.55 (q, 2H), 1.21 (t, 3H), 1.02 (t, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202873B2
出典データセットuspto-grants-2012_06
ORD IDord-e5cf9ef8eeba4791a5c43d82a63ad79c
出典メモuspto-grants-2012_06