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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417505Generated: November 3, 2026

N-bromobutanimide → HCID 86589879, compound

https://huagongshe.com/reaction/2417505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactantalpha,alpha,alpha-Trifluoro-3-nitro-o-xyleneHCID 81171—
ReactantSodium BicarbonateHCID 516892—
ReactantPerbenzoic acidHCID 523077—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 86589879HCID 86589879—

Reaction Conditions

Temperature80 °C

Reaction Steps

5.0 g (24.3 mmol) of 2-methyl-1-nitro-3-(trifluoromethyl)benzene was added to a mixture of 100 ml of benzene, 50 ml of perbenzoic acid and 5.6 g (32 mmol) of N-bromosuccinimide, and they were stirred at 80° C. for 2 days. After the treatment with ethyl acetate as the extracting solvent by an ordinary method, the obtained crude product was dissolved in 50 ml of ethanol. 6.8 g (48.6 mmol) of glycine ethyl ester hydrochloride and 6.1 g (72.9 mmol) of sodium hydrogencarbonate were added to the obtained solution, and they were stirred at 70° C. for 6 hours. The solvent was evaporated. After the extraction with ethyl acetate, the extract was washed with 1 N hydrochloric acid. The obtained aqueous layer was made basic with 1 N sodium hydroxide. After the extraction with ethyl acetate, the obtained organic layer was washed with saturated aqueous sodium chloride solution and then dried. The solvent was evaporated to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825191B2
Source datasetuspto-grants-2004_11
ORD IDord-ff61a2b9ec584bf7aca9ca9722186a64
Source noteuspto-grants-2004_11