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HRID 15705作成日:2026年10月26日

Acetic Acid → N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethyl]-N-(3,5-dimethylphenyl)amine

https://huagongshe.com/reaction/15705

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物3,5-DimethylanilineHCID 7949—
反応物Sodium borohydrideHCID 4311764—
反応物2-(2,3,4,5-Tetramethylcyclopentadienyl)benzaldehydeHCID 131727115—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethyl]-N-(3,5-dimethylphenyl)amineHCID 13172712098.1%

反応手順

To a solution of 2-(2,3,4,5-tetramethylcyclopentadienyl)benzaldehyde (15.0 mmol) in ethanol (44.6 mL) were added dropwise 3,5-dimethylaniline (15.8 mmol) and acetic acid (1.5 mmol) under a nitrogen atmosphere. The mixture was stirred at room temperature. After disappearance of the aldehyde was confirmed by gas chromatography, sodium borohydride (19.5 mmol) was added to the solution and reacted at room temperature for 3 hrs. Water and toluene were then added to the reaction mixture. The organic layer was dried and concentrated. The obtained oily substance was purified by silica gel column chromatography to give N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethyl]-N-(3,5-dimethylphenyl)amine (4.88 g, yield 73.3%) as a yellow oily substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732643B2
出典データセットuspto-grants-2010_06
ORD IDord-3e24f844693c410390771f2533932470
出典メモuspto-grants-2010_06