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HRID 77907作成日:2026年10月23日

Diethyl Ether → 4-(Hydroxy-(5-methyl-furan-2-yl)-methyl)benzaldehyde

https://huagongshe.com/ja/reaction/77907

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物5-MethylfurfuralHCID 12097—
反応物1-Bromo-4-(dimethoxymethyl)benzeneHCID 688342—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物4-(Hydroxy-(5-methyl-furan-2-yl)-methyl)benzaldehydeHCID 5925533612.3%

反応手順

To a mixture of 4-bromobenzaldehyde dimethyl acetal (2.0 mL, 12 mmol) and diethyl ether (30 mL) was added dropwise n-butyl lithium (1.6 M n-hexane solution, 9.0 mL, 14 mmol) at −78° C., which was stirred for 20 minutes at the same temperature. 5-Methylfurfural (1.3 mL, 13 mmol) was added dropwise into the reaction mixture at that temperature, and stirred for 50 minutes at 0° C. Water and ethyl acetate were added to extract the reaction mixture. The organic layer was washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:2) to obtain the title compound (320 mg, 12%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841327B2
出典データセットuspto-grants-2014_09
ORD IDord-6920c4aa6e6d497f8f26e68e053247cc
出典メモuspto-grants-2014_09