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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1287542생성일: 2026년 10월 27일

Benzyl Chloride → D-leucic acid benzyl ester

https://huagongshe.com/reaction/1287542

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl ChlorideHCID 7503—
반응물TriethylamineHCID 8471—
반응물(R)-2-hydroxy-4-methylpentanoic acidHCID 439960—
용매1,4-DioxaneHCID 31275—
생성물D-leucic acid benzyl esterHCID 9991100—

반응 단계

264.0 g. of (R)-2-hydoxy-isocaproic acid were dissolved in 1.8 liters of absolute dioxan in a three-necked flask fitted with a stirrer, thermometer and reflux condenser with a calcium chloride tube. The solution was treated successively with 285 ml. of triethylamine and 236 ml. of benzyl chloride and heated at an internal temperature of 100° for 20 hours with stirring in an oil-bath. After cooling, the resulting triethylamine hydrochloride was filtered off and washed with 500 ml. of ethyl acetate. The filtrate was evaporated under reduced pressure at 50°. The residual oil was dissolved in 800 ml. of ethyl acetate and washed twice with 150 ml. portions of 3-N hydrochloric acid, twice with 100 ml. portions of 5 percent sodium chloride solution, twice with 150 ml. portions of 10 percent potassium bicarbonate solution and twice with 100 ml. portions of 5 percent sodium chloride solution. After each of these washings, the oil was rinsed with 200 ml. of ethyl acetate. The ethyl acetate solutions were dried over magnesium sulphate and evaporated under reduced pressure at 50°. The crude product which was thus-obtained was distilled at 0.3 Torr (112°-115°). There was obtained benzyl-(R)-2-hydroxy-isocaproate; [α]D25 = + 18.0° (c = 1 in methanol); nD23 = 1.498.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE029003
출처 데이터셋uspto-grants-1976_10
ORD IDord-71f8c0e1131c448bb76e9cebf1aba55f
출처 메모uspto-grants-1976_10