戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 460020作成日:2026年10月26日

Benzyl Bromide → Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-

https://huagongshe.com/reaction/460020

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物4'-Hydroxy-3'-methylacetophenoneHCID 70135—
溶媒AcetonitrileHCID 6342—
生成物Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-HCID 12969325—

反応条件

温度40 °C

反応手順

A mixture of 4-hydroxy-3-methylacetophenone (5.0 g) in dry acetonitrile (50 ml) was treated with potassium carbonate (5.06 g) and benzyl bromide (3.96 ml) and the reaction mixture heated at 40° C. After 3 hours the reaction was allowed to cool and was concentrated. The residue was partitioned between water and ethyl acetate; the aqueous layer separated and extracted twice more with ethyl acetate. The organic solutions were combined and were dried with brine and over magnesium sulfate and concentrated to give the title compound as a colourless oil

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196107B2
出典データセットuspto-grants-2007_03
ORD IDord-da235d1cfd0447f28bdf62d1f7e867b5
出典メモuspto-grants-2007_03