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HRID 728247作成日:2026年10月26日

Butyric Acid → 2-Benzylbutanoic acid

https://huagongshe.com/reaction/728247

反応式

関与物質

役割名称HCID仕込み量
反応物Butyric AcidHCID 264—
反応物Benzyl ChlorideHCID 7503—
反応物DiisopropylamineHCID 7912—
反応物Lithium diisopropylamideHCID 2724682—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2-Benzylbutanoic acidHCID 2188177%

反応条件

温度0 °C

反応手順

Diisopropylamine (3.2 ml) was dissolved in 20 ml of tetrahydrofuran, cooled to 0° C. and treated with 14.2 ml of 1.6M n-butyllithium. After 30 minutes, the lithium diisopropylamide was added to 1 g of n-butyric acid in 75 ml of tetrahydrofuran at -78° C. After 10 minutes the reaction was warmed to -20° C. After 10 more minutes the reaction was warmed slowly to room temperature. The solution was then heated to approximately 35° C. for 30 minutes and then cooled back to room temperature and 1.3 ml of benzyl chloride was added. After 1.5 hours the reaction mixture was heated to 35° C. for 2.5 hours. The solution was then cooled, diluted with 300 ml of water, rinsed with diethyl ether (2×200 ml), and the aqueous phase was acidified with 1 M hydrochloric acid and extracted with diethyl ether (3×200 ml). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated. The residue was purified by radial chromatography (50% ethyl acetate in hexane, 2 mm plate) to yield 1.56 g of 2-benzylbutyric acid (77% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05047534
出典データセットuspto-grants-1991_09
ORD IDord-fe565d64ee064018b1ce702af2b6474b
出典メモuspto-grants-1991_09