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HRID 258820作成日:2026年10月27日

4-Nitrobenzyl chloride → 4-{[4-(Diphenylmethyl)-1-piperidinyl]methyl}benzenamine

https://huagongshe.com/reaction/258820

反応式

関与物質

役割名称HCID仕込み量
反応物4-Nitrobenzyl chlorideHCID 7482—
反応物Sodium CarbonateHCID 10340—
反応物4-BenzhydrylpiperidineHCID 88278—
反応物4-(Diphenylmethyl)-1-[(4-nitrophenyl)methyl]piperidineHCID 21424840—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物4-{[4-(Diphenylmethyl)-1-piperidinyl]methyl}benzenamineHCID 20225820—

反応手順

The basic primary amine of this invention can be prepared by heating 4-(diphenylmethyl)piperidine with 4-nitrobenzyl chloride in the presence of sodium carbonate, using ethanol and water as solvents, and contacting the resultant 1-[(4-nitrophenyl)methyl]-4-(diphenylmethyl)piperidine in tetrahydrofuran solution at 25° with hydrogen under approximately 0.1 atm of pressure, using 5% palladium-on-charcoal as catalyst. From 4-{[4-(diphenylmethyl)-1-piperidinyl]methyl}benzenamine thus or otherwise produced, on heating in acetic acid solution with an alkanoic acid anhydride, a corresponding basic N-alkanoyl amine of this invention can be prepared. And by heating a dichloromethane solution of 4-(diphenylmethyl)piperidine and 4-[(alkylamino)/(dialkylamino)]benzoic acid in the presence of N,N1 -methanetetraylbiscyclohexanamine, then heating the resultant amide with lithium tetrahydroaluminate(1-) in tetrahydrofuran, a corresponding basic N-alkyl or N,N-dialkyl amine of this invention can be prepared.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04035372
出典データセットuspto-grants-1977_07
ORD IDord-07f3a93d72e64b0d82d8deca20c384b3
出典メモuspto-grants-1977_07