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HRID 743387作成日:2026年10月25日

Benzyl 2-[4-(2-methoxyphenyl)-1-butenyl]phenyl ether → 2-[4-(2-Methoxyphenyl)butyl]phenol

https://huagongshe.com/reaction/743387

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl 2-[4-(2-methoxyphenyl)-1-butenyl]phenyl etherHCID 67667339—
溶媒EthanolHCID 702—
溶媒PalladiumHCID 23938—
溶媒HCID 178418361HCID 178418361—
生成物2-[4-(2-Methoxyphenyl)butyl]phenolHCID 1942397960%

反応手順

Following a procedure similar to that described in the latter part of Preparation 3, the whole of the benzyl 2-[4-(2-methoxyphenyl)-1-butenyl]phenyl ether prepared as described above was dissolved in 50 ml of ethanol and hydrogenated at 50° C. in an atmosphere of hydrogen at atmospheric pressure and in the presence of 100 mg of 5% w/w palladium-on-charcoal for 6 hours. The crude product thus obtained was purified by column chromatography through silica gel, using 10:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 0.44 g (yield 60%) of the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05556864
出典データセットuspto-grants-1996_09
ORD IDord-2b23264ec9294908b1df8c2d52871c46
出典メモuspto-grants-1996_09