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HRID 220472생성일: 2026년 10월 25일

Ethyl bromoacetate → 3-Acetyl-6-methyl-4-oxoheptanoic acid ethyl ester

https://huagongshe.com/reaction/220472

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물Sodium hydrideHCID 24758—
반응물2,4-Heptanedione, 6-methyl-HCID 76354—
용매TetrahydrofuranHCID 8028—
생성물3-Acetyl-6-methyl-4-oxoheptanoic acid ethyl esterHCID 8664165173%

반응 단계

Add a solution of 6-methylheptane-2,4-dione (5.0 g, 35.16 mmol) in tetrahydrofuran (50 mL) dropwise to a cooled suspension (0° C.) of sodium hydride (1.69 g, 42.2 mmol, 60% dispersion in oil) in tetrahydrofuran (50 mL). After 1 hr., add bromoacetic acid ethyl ester (4.28 mL, 38.68 mmol) dropwise and stir at 0° C. to room temperature over 88 hr. Partition the reaction mixture between ethyl acetate (200 mL) and saturated aqueous ammonium chloride solution (100 mL). Separate the organic layer, dry (sodium sulfate), filter and concentrate. Purify using silica gel chromatography (95:5 hexanes:ethyl acetate) to give 3-acetyl-6-methyl-4-oxoheptanoic acid ethyl ester (5.81 g, 73%). 1H-NMR (400 MHz, CDCl3) δ 4.10 (m, 4H), 2.81 (d, 2H), 2.41 (t, 1H), 2.22 (s, 3H), 1.23 (m, 4H), 0.92 (m, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202873B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-a89542bd527947c79ea97fb83ad6b93d
출처 메모uspto-grants-2012_06