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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410306Generated: November 1, 2026

Dimethylformamide → HCID 3126580, compound

https://huagongshe.com/reaction/2410306

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 stifling. 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 numberUS08816089B2
Source datasetuspto-grants-2014_08
ORD IDord-6975e246e2bc404988af9841687b7ef9
Source noteuspto-grants-2014_08