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HRID 563662作成日:2026年10月25日

Benzyl Bromide → Ethyl 2-(4-(benzyloxy)-3-bromophenyl)acetate

https://huagongshe.com/reaction/563662

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Ethyl 2-(3-bromo-4-hydroxyphenyl)acetateHCID 18620106—
溶媒AcetonitrileHCID 6342—
生成物Ethyl 2-(4-(benzyloxy)-3-bromophenyl)acetateHCID 18620085—

反応手順

To a suspension of (3-bromo-4-hydroxy-phenyl)-acetic acid ethyl ester (0.100 g, 0.39 mmol) and cesium carbonate (0.376 g, 1.16 mmol) in MeCN was added benzyl bromide (0.06 mL, 0.46 mmol), and the reaction was stirred at room temperature until no starting material was seen by analytical tlc. The mixture was partitioned between EtOAc and H2O, and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, and concentrated to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067445B2
出典データセットuspto-grants-2011_11
ORD IDord-3a0aa6086fd9412c80c875c8103a2250
出典メモuspto-grants-2011_11