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HRID 1625998作成日:2026年10月25日

Benzyl Bromide → benzyl 5-bromo-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1625998

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1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物5-Bromo-1H-indole-2-carboxylic acidHCID 252137—
溶媒AcetonitrileHCID 6342—
生成物benzyl 5-bromo-1H-indole-2-carboxylateHCID 67077949—

反応手順

Benzyl bromide (160 μl) and 1,8-diazabicyclo[5.4.0]undec-7-ene (201 μl) were added to a solution of 5-bromo-1H-indole-2-carboxylic acid (161 mg) in acetonitrile (3.5 ml) at room temperature, followed by stirring for 22.5 hours. The reaction solution was concentrated and separated by adding ethyl acetate and distilled water. The resulting organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The resulting residue was solidified from dichloromethane-hexane, collected by filtration and washed with hexane. This was dried under reduced pressure to give the title compound (189 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08785438B2
出典データセットuspto-grants-2014_07
ORD IDord-0681cde35a654fa7be887a086c549c18
出典メモuspto-grants-2014_07