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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | 3,5-Dimethylaniline | HCID 7949 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 2-(2,3,4,5-Tetramethylcyclopentadienyl)benzaldehyde | HCID 131727115 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethyl]-N-(3,5-dimethylphenyl)amine | HCID 131727120 | 98.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07732643B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-3e24f844693c410390771f2533932470 |
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| 출처 메모 | uspto-grants-2010_06 |
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