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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257176Generated: November 1, 2026

2,4,6-Trifluoroaniline → HCID 14995455, compound

https://huagongshe.com/reaction/2257176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrifluoroanilineHCID 67765—
ReactantHCID 14995454HCID 14995454—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 14995455HCID 1499545558.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656634
Source datasetuspto-grants-1997_08
ORD IDord-3ac37939e9c74628b2648c3f1d34aff8
Source noteuspto-grants-1997_08