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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15705생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/15705

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물3,5-DimethylanilineHCID 7949—
반응물Sodium borohydrideHCID 4311764—
반응물2-(2,3,4,5-Tetramethylcyclopentadienyl)benzaldehydeHCID 131727115—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethyl]-N-(3,5-dimethylphenyl)amineHCID 13172712098.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732643B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3e24f844693c410390771f2533932470
출처 메모uspto-grants-2010_06