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HRID 26084作成日:2026年10月26日

Dimethylformamide → 3-(Benzyloxy)-4-bromophenol

https://huagongshe.com/reaction/26084

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Benzyl BromideHCID 7498—
反応物4-BromoresorcinolHCID 81105—
反応物Potassium hydrideHCID 82127—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物3-(Benzyloxy)-4-bromophenolHCID 15670654—

反応条件

温度0 °C

反応手順

To a 0° C. slurry of 1.7 g. (42.5 mmoles) of potassium hydride in 35 ml. of N,N-dimethylformamide is slowly added a solution of 7.22 g. (38.2 mmoles) of 4-bromoresorcinol. The resultant mixture is stirred for 30 minutes and then 4.54 ml. (38.2 mmoles) of benzyl bromide is slowly added. The reaction mixture is stirred 3 hours longer at 0° C. and then added to 200 ml. of cold water and 200 ml. of ether. The ether extract is washed twice with 200 ml. portions of water, dried over magnesium sulfate and evaporated to an oil. The crude oil is purified via column chromatography on 400 g. of silica gel eluted with 25% ether-pentane to yield (in order of elution) 2.2 g. (16%) of 2,4-dibenzyloxybromobenzene, 0.21 g. (2%) of 5-benzyloxy-2-bromophenol and 3.52 g. (33%) of 3-benzyloxy-4-bromophenol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04147872
出典データセットuspto-grants-1979_04
ORD IDord-cbaf3fd342894c14a78febb86ca2b7a8
出典メモuspto-grants-1979_04