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HRID 1584338생성일: 2026년 10월 27일

Hexane → Ethyl 7-[3-methoxy-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]heptanoate

https://huagongshe.com/reaction/1584338

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물(5-Ethoxycarbonylpentyl)triphenylphosphonium bromideHCID 10345271—
반응물3-Methoxy-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzaldehydeHCID 10829743—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 7-[3-methoxy-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]heptanoateHCID 2122441985%

반응 단계

To a suspension of (5-ethoxycarbonylpentyl)triphenylphosphonium bromide (3.0 g) in tetrahydrofuran (THF) (70 ml) was added dropwise, in nitrogen streams at -30° C., a hexane solution of n-butyl lithium (1.6M, 3.9 ml). The mixture was stirred for 30 minutes at the same temperature, to which was added dropwise at -30° C. a solution of 3-methoxy-4-[5-methyl-2-phenyl-4-oxazolylmethoxy)benzaldehyde (1.0 g) in tetrahydrofuran (THF) (10 ml). The mixture was stirred for 4 hours at temperature ranging from 50 to 60° C. The reaction mixture was then poured into water, which was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), followed by distilling off the solvent under reduced pressure. The residue was subjected to column chromatography on silica gel. From the fraction eluted with ethyl acetate-hexane (1:4), was obtained ethyl 7-[3-methoxy-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]heptanoate (9.7 g, 85%) as an oily product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05932601
출처 데이터셋uspto-grants-1999_08
ORD IDord-2c8c9a3a63424b8f92e3be6d51f1ccfe
출처 메모uspto-grants-1999_08