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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099106Generated: November 2, 2026

Dimethylformamide → HCID 3126580, compound

https://huagongshe.com/reaction/2099106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantIndolineHCID 10328—
Reactant4-Fluoro-3-nitrobenzotrifluorideHCID 67778—
ReactantDiisopropylethylamineHCID 81531—
SolventWaterHCID 962—
ProductHCID 3126580HCID 312658099.4%

Reaction Steps

Indoline (402 μl, 3.59 mmol, commercially available product) and N,N-diisopropylethylamine (619 μl, 3.59 mmol) were sequentially added at 0° C. to a N,N-dimethylformamide (DMF; 2 ml) solution of 1-fluoro-2-nitro-4-(trifluoromethyl)benzene (498 mg, 2.38 mmol, commercially available product). The resulting mixture was warmed to room temperature and stirred for one hour. The mixture was then heated at 70° C. for 5.5 hours with stirring. The mixture was cooled to room temperature. Water was added to the mixture, and the resulting mixture was extracted three times with ethyl acetate. The obtained organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (30 g, hexane/ethyl acetate=20/1). Thus, 1-(2-nitro-4-(trifluoromethyl)phenyl)indoline (730 mg, 99.4%) was yielded as a deep red oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569536B2
Source datasetuspto-grants-2009_08
ORD IDord-09012c1ae0d7453ba4fb4a7118dd8f3b
Source noteuspto-grants-2009_08