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HRID 27146作成日:2026年10月26日

1-Butanol → 1-(N-benzyloxycarbonyl-p-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

https://huagongshe.com/reaction/27146

反応式

関与物質

役割名称HCID仕込み量
反応物1-ButanolHCID 263—
反応物Dopamine HydrochlorideHCID 65340—
反応物N-benzyloxycarbonyl-p-fluoroanilinoacetaldehyde diethyl acetalHCID 20460532—
溶媒WaterHCID 962—
生成物1-(N-benzyloxycarbonyl-p-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 2046054244.6%

反応手順

N-benzyloxycarbonyl-p-fluoroanilinoacetaldehyde diethyl acetal (6 g) and 3,4-dihydroxyphenethylamine hydrochloride (2.5 g) were added to a mixture of n-butyl alcohol (60 ml) and water (8.5 ml). The mixture was then refluxed for 11 hours in a stream of nitrogen. In the course of the reaction, amounts of the above-mentioned acetal (0.6 g and 1.2 g) were added to the mixture after 4.5 hours and 6 hours, respectively, from the beginning of the reaction. The reaction mixture was concentrated to dryness and the residue was washed with ether and dissolved in water. The solution was washed with ether and concentrated to dryness to give amorphous 1-(N-benzyloxycarbonyl-p-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (2.7 g), mp 122° C. (dec.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04220647
出典データセットuspto-grants-1980_09
ORD IDord-5ff7cb659ce54ae3ac8a4d37277a9d40
出典メモuspto-grants-1980_09