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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2352116생성일: 2026년 10월 26일

Diisopropylamine → Methyl 2-methoxy-3-hydroxy-3-(2-dodecylphenyl)propionate

https://huagongshe.com/reaction/2352116

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물Methyl methoxyacetateHCID 80507—
반응물2-DodecylbenzaldehydeHCID 14097572—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-methoxy-3-hydroxy-3-(2-dodecylphenyl)propionateHCID 15617501—

반응 단계

To a solution of di-i-propylamine (0.77 ml, 5 mmoles) in tetrahydrofuran (10 ml) at -78° C. was added n-butyl lithium (2.1 ml, 5.5 mmoles) under argon atmosphere. After 15 minutes, methyl methoxyacetate (0.52 g, 5 mmoles) in tetrahydrofuran (2 ml) was added dropwise, with stirring. The resulting enolate solution was stirred at -78° C. for 45 minutes. A solution of 2-dodecylbenzaldehyde (1.65 g, 6 mmoles) in tetrahydrofuran (2 ml) was added. The resulting light-blue mixture became a suspension after 1.5 hours. The reaction mixture was quenched with saturated ammonium chloride solution, diluted with ether and ice-water. The aqueous phase was extracted with ether. The combined organic extract was washed with saturated sodium chloride solution, dried over magnesium sulfate, and evaporated to give the product, which was purified by flash column chromatography (silica, 15% ethyl acetate/hexane). The fractions were pooled to give 620 mg (33%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04874792
출처 데이터셋uspto-grants-1989_10
ORD IDord-ebf4bba9fdb84dedb704c03ee6b125e8
출처 메모uspto-grants-1989_10