Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 913826Erstellt: 26. Oktober 2026

Acetic Acid → 2-Bromo-4-chloro-6-methylbenzenamine

https://huagongshe.com/reaction/913826

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt4-Chloro-2-toluidineHCID 7251—
EduktPotassium BromideHCID 253877—
EduktSodium BicarbonateHCID 516892—
EduktSodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
KatalysatorAmmonium paramolybdate tetrahydrateHCID 16211167—
LösungsmittelWaterHCID 962—
Produkt2-Bromo-4-chloro-6-methylbenzenamineHCID 20543754—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4-Chloro-2-methylaniline (1.0 g, 7.06 mmol), potassium bromide (1.01 g, 8.47 mmol), and ammonium heptamolybdate tetrahydrate (87 mg, 0.07 mmol) were suspended in acetic acid (7 mL, 122 mmol) and cooled to 0° C. The reaction was treated with sodium perborate tetrahydrate (1.2 g, 7.77 mmol), stirred at 0° C. for 30 min, and at room temperature for 2 h. The mixture was poured into water, neutralized with saturated sodium bicarbonate and extracted with ethyl acetate (2×). The organic layers were pooled together, washed with brine (2×), dried over sodium sulfate, and concentrated to afford 1.2 g (78%). 1H-NMR (CDCl3, 500 MHz) δ 7.28 (s, 1H), 6.97 (s, 1H), 4.03 (bs, 2H), 2.17 (s, 3) Mass spec.: 221.90 (MH)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08026257B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-b3bb722067144d10a04789b67aeacb86
Quellennotizuspto-grants-2011_09