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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356878생성일: 2026년 10월 26일

Butyric Acid → 2-Benzylbutanoic acid

https://huagongshe.com/reaction/356878

반응식

참여 물질

역할이름HCID투입량
반응물Butyric AcidHCID 264—
반응물Benzyl ChlorideHCID 7503—
반응물DiisopropylamineHCID 7912—
반응물Lithium diisopropylamideHCID 2724682—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-Benzylbutanoic acidHCID 2188177%

반응 조건

온도0 °C

반응 단계

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 1M 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840729
출처 데이터셋uspto-grants-1998_11
ORD IDord-7ad15992cd63445d9e1a2caa52f81924
출처 메모uspto-grants-1998_11