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HRID 844950作成日:2026年10月24日

Dichloroacetyl chloride → 2-(Dichloroacetyl)-1-(1-methylethyl)-4-methyl-1,2,3,4-tetrahydro-isoquinoline

https://huagongshe.com/ja/reaction/844950

反応式

関与物質

役割名称HCID仕込み量
反応物Dichloroacetyl chlorideHCID 6593—
反応物IsoquinolineHCID 8405—
反応物2-PhenylpropylamineHCID 11398—
反応物Sodium HydroxideHCID 14798—
反応物Isobutyryl chlorideHCID 62325—
反応物4-Methyl-1,2,3,4-tetrahydroisoquinolineHCID 13738934—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-(Dichloroacetyl)-1-(1-methylethyl)-4-methyl-1,2,3,4-tetrahydro-isoquinolineHCID 20133043—

反応手順

By procedures described in Example 1 (Method A), β-methyl-phenethylamine and isobutyryl chloride were converted to -4-methyl-1,2,3,4-tetrahydroisoquinoline. A reaction vessel was charged with 3.0 g of this isoquinoline compound, 10 ml 10% sodium hydroxide and 50 ml methylene chloride. With this mixture stirred, 2 ml dichloroacetyl chloride was added dropwise to the mixture. The mixture was stirred for 2 minutes, then water was added. The organic extract was dried with magnesium sulfate and stripped of solvent. The residue was recrystallized from aqueous ethanol to provide 4 g of a white needle-crystalline product having the elemental analysis reported in Table I.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04755218
出典データセットuspto-grants-1988_07
ORD IDord-451cd1213c07448ab4fd623420318f8e
出典メモuspto-grants-1988_07