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HRID 1584338作成日:2026年10月25日

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

https://huagongshe.com/reaction/1584338

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物(5-Ethoxycarbonylpentyl)triphenylphosphonium bromideHCID 10345271—
反応物3-Methoxy-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzaldehydeHCID 10829743—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 7-[3-methoxy-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]heptanoateHCID 2122441985%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05932601
出典データセットuspto-grants-1999_08
ORD IDord-2c8c9a3a63424b8f92e3be6d51f1ccfe
出典メモuspto-grants-1999_08