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HRID 849708作成日:2026年10月23日

Diethyl Oxalate → Ethylcyclohexyl(oxo)acetate

https://huagongshe.com/ja/reaction/849708

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl OxalateHCID 7268—
反応物HCID 178419651HCID 178419651—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Ethylcyclohexyl(oxo)acetateHCID 1104140786%

反応条件

温度0 °C

反応手順

Cyclohexyl magnesium bromide (Aldrich) in ether (2 M, 150 mL) was pumped under vacuum to remove ethyl ether, at rt, the residue obtained was then dissolved in anhydrous THF (100 mL) while cooled with an ice water bath. The solution was then added to a solution of diethyl oxalate (60 g) in THF (150 mL) at -30--40° C. in 10 min. The reaction mixture was warmed to 0° C. for 5 min, and quenched with 10% HCl (100 mL), extracted with ethyl acetate (200 mL), the extract was washed with water (30 mL), brine (50 mL) and dried with sodium sulfate, then filtered. The filtrate was concentrated to give an oil. It was distilled 40-50° C. at 1 mm Hg to remove the starting material and the left over is the product (total of 46 g, 86% yield, purity>90%, it can be distilled at 1 mm Hg, 75-80° C.): 1H NMR δ 1.20-1.40 (m, 8H), 1.62-1.94 (m, 5H), 3.02 (broad s, 1H), 4.30 (q, J=8 Hz, 2H). 13C-NMR δ 13.91, 25.11, 25.58, 27.36, 46.13, 62.07, 161.84, 197.51.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06013830
出典データセットuspto-grants-2000_01
ORD IDord-55e388e290ef4699a19fcc74d966fce0
出典メモuspto-grants-2000_01