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HRID 270929作成日:2026年10月26日

Benzyl Bromide → Methyl 2-(4-benzyloxyphenyl)acetate

https://huagongshe.com/reaction/270929

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Cesium carbonateHCID 10796—
反応物Benzeneacetic acid, 4-hydroxy-, methyl esterHCID 518900—
溶媒DimethylformamideHCID 6228—
生成物Methyl 2-(4-benzyloxyphenyl)acetateHCID 275664583%

反応手順

A solution of 15 g (90.3 mmol) of methyl 4-hydroxyphenylacetate in 25 mL of dimethylformamide (DMF) was added 32.4 g (99.3 mmol) of cesium carbonate, followed by 13.4 mL (112.9 mmol) of benzyl bromide (BnBr), and the resulting heterogeneous mixture was stirred at rt for 72 h. The reaction mixture was filtered, the solids were washed with ethyl acetate, and the combined organic extracts were concentrated to give a residue which was chromatographed on silica gel (25% hexane in dichloromethane) to afford 19.1 g (83% yield) of desired (4-benzyloxy-phenyl)-acetic acid methyl ester as indicated by 1H NMR; LC-MS—calcd for C16H16O3 [M++H]+: 257.11, found: 257.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449488B2
出典データセットuspto-grants-2008_11
ORD IDord-a54f2345cbbd4689a0409ce090346a3a
出典メモuspto-grants-2008_11