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HRID 1505043作成日:2026年10月27日

Water → 1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-one

https://huagongshe.com/reaction/1505043

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物ChloroacetoneHCID 6571—
反応物Potassium CarbonateHCID 11430—
反応物5-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 45074003—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-oneHCID 58318043—

反応手順

A mixture containing 5-bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride (1 g, 4 mmol), chloroacetone (407 mg, 4.4 mmol) and potassium carbonate (1.38 g, 10 mmol) in dimethyl formamide (DMF) (8 ml) is stirred at room temperature for 18 hours. To this mixture is added water (50 ml) and ethyl acetate (50 ml). The organic layer is separated, washed with brine, dried over MgSO4, and concentrated. The crude product is purified by flash column chromatography using 30% ethyl acetate in dichloromethane as eluent to give 1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-one as an orange oil. LC-MS m/z: 269.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09216964B2
出典データセットuspto-grants-2015_12
ORD IDord-fa029e8b621649dc8a8aca503df3aa64
出典メモuspto-grants-2015_12