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HRID 551776作成日:2026年10月27日

Butylate → 7-Methoxy-1-vinylnaphthalene

https://huagongshe.com/reaction/551776

反応式

関与物質

役割名称HCID仕込み量
反応物ButylateHCID 16181—
反応物PotassiumHCID 5462222—
反応物2-(7-Methoxynaphthalen-1-yl)ethyl methanesulfonateHCID 19085990—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物7-Methoxy-1-vinylnaphthaleneHCID 44541668—

反応手順

The compound obtained in Step A (21.4 mmol) is dissolved in 120 ml of tetrahydrofuran, and potassium tent-butylate (64.2 mmol) is added in small portions. After stirring for 30 minutes at ambient temperature, the reaction mixture is evaporated to dryness. The residue obtained is taken up in 150 ml of water and the aqueous phase is extracted twice with 60 ml of diethyl ether. The organic phase is washed with water, dried over magnesium sulphate, decolourised on vegetable carbon and evaporated. The residue obtained is purified on silica gel (eluant: petroleum ether) to yield the title product in the form of a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947852B2
出典データセットuspto-grants-2011_05
ORD IDord-c307d8c7baac4019b1c29cce6b41bdff
出典メモuspto-grants-2011_05