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HRID 1031245作成日:2026年10月24日

1-Bromo-2-methylpropane → 2-Isobutyl-3-ketoglutarate diethyl ester

https://huagongshe.com/ja/reaction/1031245

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-2-methylpropaneHCID 6555—
反応物Diethyl acetonedicarboxylateHCID 66045—
反応物Magnesium ethanolateHCID 164963—
生成物2-Isobutyl-3-ketoglutarate diethyl esterHCID 999265962%

反応手順

Diethyl 3-oxopentanedioate (45.5 ml, 0.25 mol) was added to a suspension of magnesium ethoxide (prepared from magnesium turnings (9 g, 0.375 mol) and iodine (0.1 g) in dry ethanol (275 ml)), and the mixture was heated under reflux for 90 min. 1-Bromo-2-methylpropane (54 ml, 0.5 mol) was added, and the reaction was heated under reflux for 16 h. Further 1-bromo-2-methylpropane (27 ml, 0.25 mol) was added to the boiling mixture, and after 3 h the solvent was evaporated in vacuo. The residue was partitioned between 2 N hydrochloric acid and ether. After extracting the aqueous phase with ether, the combined organics were washed successively with water, 5% sodium bicarbonate, water and brine, then were dried (Na2SO4) and evaporated in vacuo. The residue was distilled to give the title compound as a colourless oil (40 g, 62%), bp 118°-120° C. (1 mmHg). δ (CDCl3): 0.9 (6H, d, J=6Hz), 1.25 (6H, t, J=7Hz), 1.4-1.9 (3H, m), 3.5 (2H, s), 3.7 (1H, d, J=9Hz) and 4.2 (4H, q, J=7Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05109000
出典データセットuspto-grants-1992_04
ORD IDord-9f409073cecb4cee984edb22c535e47b
出典メモuspto-grants-1992_04