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HRID 26479作成日:2026年10月26日

Phenethyl bromide → N-Phenethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline

https://huagongshe.com/reaction/26479

反応式

関与物質

役割名称HCID仕込み量
反応物Phenethyl bromideHCID 7666—
反応物PentaneHCID 8003—
反応物Sodium hydrideHCID 24758—
反応物4a-(m-Methoxyphenyl)-1,3-diketo-trans-decahydroisoquinolineHCID 86736478—
溶媒DimethylformamideHCID 6228—
生成物N-Phenethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinolineHCID 13282015—

反応手順

A solution of 10.0 g (37 mmoles) of 4a-(m-methoxyphenyl)-1,3-diketo-trans-decahydroisoquinoline in 250 ml of anhydrous dimethylformamide was added with stirring to a suspension of 2.8 g (55.5 mmoles) of 50% sodium hydride in mineral oil (washed with pentane) in 125 ml of anhydrous dimethylformamide heated at 50° under nitrogen. The mixture was heated at 90° for 2 hours, then cooled to 40°, at which time a solution of 14.0 g (74 mmoles) of phenethyl bromide in 20 ml of anhydrous dimethylformamide was added and the reaction mixture heated at 90° overnight. The cooled solution was poured into ice-water and extracted with ether. Evaporation of the ether gave an oil which was purified by column chromatography (Silicar CC-7, eluting with acetone-benzene). The major fraction was identified as N-phenethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04150135
出典データセットuspto-grants-1979_04
ORD IDord-39d377ee3df3459fbf811c3daf211de4
出典メモuspto-grants-1979_04