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HRID 2167835作成日:2026年10月27日

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

https://huagongshe.com/reaction/2167835

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AcetoneHCID 180—
生成物Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-HCID 1296932599.1%

反応手順

A mixture of 4′-hydroxy-3′-methylacetophenone (10.00 g; 66.6 mmol) and K2CO3 (13.80 g; 99.9 mmol) in acetone (100 mL) was stirred, at RT for 40 minutes. Subsequently, benzyl bromide (7.9 mL; 66.6 mmol) was added and the resulting mixture was heated under reflux for 2.5 h. After cooling to RT the mixture was concentrated in vacuo. The residue was dissolved in EtOAc, washed with 5% aqueous ammonia, water, and brine, dried (MgSO4), filtered and concentrated in vacuo to afford 1-(4-benzyloxy-3-methylphenyl)-ethanone (15.86 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09045441B2
出典データセットuspto-grants-2015_06
ORD IDord-eee07cea7e334acc82d58ad89ec6569c
出典メモuspto-grants-2015_06