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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470963Generated: November 2, 2026

4-(Trifluoromethyl)aniline → HCID 67236836, compound

https://huagongshe.com/reaction/1470963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)anilineHCID 9964—
Reactant1,4-Bis(4-bromophenyl)butane-1,4-diyl dimethanesulfonateHCID 58226531—
SolventDimethylformamideHCID 6228—
ProductHCID 67236836HCID 67236836—

Reaction Conditions

Temperature50 °C

Reaction Steps

The product from Example 42B (11.13 g, 20.0 mmol) and 4-(trifluoromethyl)aniline (32.2 g, 200 mmol) were combined in DMF (50 mL). The mixture was stirred at 50° C. under nitrogen overnight. The reaction mixture was evaporated and the residue was diluted with ethyl acetate, treated with 1M HCl, stirred for 10 minutes, and filtered to remove the solid. The organic layer of filtrate was washed with brine, dried with sodium sulfate, filtered and evaporated. The residue was purified by chromatography on silica gel eluting with ethyl acetate/hexane (0 to 1%). The title compounds (500 mg, 5%) were eluted as the first of 2 stereoisomers and were obtained as a mixture of trans diastereomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006387B2
Source datasetuspto-grants-2015_04
ORD IDord-b634bd9ca0da468f8d827df0d6bb7d5f
Source noteuspto-grants-2015_04