HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15705Generated: October 26, 2026
Acetic Acid → N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethyl]-N-(3,5-dimethylphenyl)amine
https://huagongshe.com/reaction/15705
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3,5-Dimethylaniline | HCID 7949 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(2,3,4,5-Tetramethylcyclopentadienyl)benzaldehyde | HCID 131727115 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethyl]-N-(3,5-dimethylphenyl)amine | HCID 131727120 | 98.1% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732643B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-3e24f844693c410390771f2533932470 |
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| Source note | uspto-grants-2010_06 |
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