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HRID 234255作成日:2026年10月26日

Water → (Z)-5-Acetylamino-2,4,6,7-tetramethyl-2-styryl-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/234255

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物5-Acetylamino-2-formyl-2,4,6,7-tetramethyl-2,3-dihydrobenzofuranHCID 19078578—
反応物HCID 178418244HCID 178418244—
触媒Benzyltriphenylphosphonium chlorideHCID 70671—
溶媒TetrahydrofuranHCID 8028—
生成物(Z)-5-Acetylamino-2,4,6,7-tetramethyl-2-styryl-2,3-dihydrobenzofuranHCID 6767145077.2%

反応条件

温度-20 °C

反応手順

A suspension of benzyltriphenylphosphonium chloride (0.7 g, 1.8 mmol) in tetrahydrofuran (10 ml) was cooled to -20° C. and n-butyllithium hexane solution (1.6M, 1.12 ml, 1.8 mmol) was added dropwise. The reaction mixture was stirred for 30 minutes and then a solution of 5-acetylamino-2-formyl-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran (0.45 g, 1.7 mmol) in tetrahydrofuran (5 ml) was added. The reaction mixture was stirred at room temperature for additional 30 minutes. Water was added to the reaction mixture and the product was extracted with ethyl acetate. The extract was washed with water, dried and then concentrated. The residue was purified by column chromatography on silica gel (isopropyl ether-ethyl acetate, 1:1) to obtain the desired compound (0.44 g, yield: 76.2%) as oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05594154
出典データセットuspto-grants-1997_01
ORD IDord-58df597f495940dda9f2b60e6efab7b3
出典メモuspto-grants-1997_01