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HRID 274039作成日:2026年10月24日

4-Hydroxybenzyl Alcohol → 4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)phenol

https://huagongshe.com/ja/reaction/274039

反応式

関与物質

役割名称HCID仕込み量
反応物4-Hydroxybenzyl AlcoholHCID 125—
反応物WaterHCID 962—
反応物PyridineHCID 1049—
反応物3-Tert-butyl-4-methoxybenzoyl chlorideHCID 13633555—
溶媒TetrahydrofuranHCID 8028—
生成物4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)phenolHCID 21474530—

反応手順

1.24 g (0.01 mol) of 4-hydroxybenzenemethanol, 1 ml (0.01 mol) of pyridine and 50 ml of THF are introduced into a round-bottomed flask. While cooling in an icebath, a solution of 2.2 g (0.01 mol) of 3-tert-butyl-4-methoxybenzoyl chloride in 50 ml of THF is introduced dropwise and the mixture is stirred at room temperature for 24 h. The reaction medium is poured into water, the mixture is extracted with ethyl ether and the organic phase is separated after settling has taken place, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column and eluted with a mixture of dichloromethane and ethyl ether (97:3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05387594
出典データセットuspto-grants-1995_02
ORD IDord-6f43e7ba229e4366a2732b9a84ac901f
出典メモuspto-grants-1995_02