HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379616Generated: October 31, 2026
2,4,6-Trifluoroaniline → HCID 14995455, compound
https://huagongshe.com/reaction/2379616
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,6-Trifluoroaniline | HCID 67765 | — |
| Reactant | HCID 14995454 | HCID 14995454 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14995455 | HCID 14995455 | 58.3% |
Reaction Steps
To a solution of 1.0 g (6.8 mmole) 2,4,6-trifluoroaniline and 830 mg (6.8 mmole) 4-dimethylaminopyridine in 40 ml methylene chloride cooled to 5° C. under nitrogen was added a solution of 2.12 g (6.6 mmole) 2-n-nonyl-1,2,3,4-tetrahydro-2-naphthoyl chloride in 10 ml methylene chloride. The resulting solution was stirred at room temperature for 44 hours. Fifty milliters of methylene chloride was then added and the solution was washed sequentially with 30 ml aqueous hydrochloric acid, 30 ml water and 30 ml brine. The methylene chloride solution was dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The residue (2.5 g) was purified by column chromatography on silica gel eluting with 2:1 methylene chloride-hexane to yield 1.66 g (58% yield) of the desired product as a white, low melting solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05362878 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-030313bb7de044aba5eece143821be70 |
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| Source note | uspto-grants-1994_11 |
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