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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1009219Erstellt: 25. Oktober 2026

Trifluoroacetic acid → 3-Bromo-N-methylaniline

https://huagongshe.com/reaction/1009219

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktSodium BicarbonateHCID 516892—
EduktN-BOC-N-Methyl-3-bromoanilineHCID 22997148—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Bromo-N-methylanilineHCID 701829990,6%

Reaktionsschritte

3.6 g (12.7 mmol) of tert-butyl (3-bromophenyl)-N-methylcarbamate, prepared in a manner analogous to Example 1b), are dissolved in 15 ml of dichloromethane. 5 ml of trifluoroacetic acid are added and the reaction mixture is stirred at ambient temperature for 1 hour. The reaction is halted by the addition of 50 ml of a saturated sodium hydrogencarbonate solution and then extraction is carried out with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated and then the residue is chromatographed on silica gel (heptane/ethyl acetate 50/50). 2.14 g of 3-bromo-N-methylaniline are obtained in the form of an oil. Yield=90%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07973063B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-68547b459c8d4acb9f3337b270c7cb90
Quellennotizuspto-grants-2011_07