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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273327Generated: October 26, 2026

N-bromobutanimide → (2-Bromo-6-nitro-4-trifluoromethyl-phenyl)-methyl-amine

https://huagongshe.com/reaction/2273327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantBenzenamine, N-methyl-2-nitro-4-(trifluoromethyl)-HCID 88405—
ReactantSodium BicarbonateHCID 516892—
SolventAcetonitrileHCID 6342—
Product(2-Bromo-6-nitro-4-trifluoromethyl-phenyl)-methyl-amineHCID 6887892269%

Reaction Steps

To a mixture of methyl-(2-nitro-4-trifluoromethyl-phenyl)-amine (16 g) and acetonitrile (200 ml) was added N-bromosuccinimide (15 g) while ice-cooling. The reaction mixture was stirred at room temperature for 5 hours. To the resulting reaction mixture was poured saturated aqueous sodium hydrogen carbonate solution, and then the mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give (2-bromo-6-nitro-4-trifluoromethyl-phenyl)-methyl-amine (15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120823B2
Source datasetuspto-grants-2015_09
ORD IDord-f4d5370820b64331a0b24e343d18aeb2
Source noteuspto-grants-2015_09