Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59586Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Bromo-4-chloro-1-(1-methylethyl)benzene

https://huagongshe.com/de/reaction/59586

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt3-Bromo-4-isopropylanilineHCID 280799—
EduktSodium NitriteHCID 23668193—
KatalysatorSulfamic AcidHCID 5987—
KatalysatorCuprous chlorideHCID 62652—
LösungsmittelWaterHCID 962—
Produkt2-Bromo-4-chloro-1-(1-methylethyl)benzeneHCID 6798828262,3%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

Hydrochloric acid (152 g, 31% strength, 1.29 mol) was added dropwise to a suspension of 3-bromo-4-isopropylaniline (VII) (100 g, 0.43 mol) and water (150 g) at room temperature. The suspension was subsequently cooled to 5° C. and a solution of sodium nitrite (32.7 g, 0.46 mol) in water (140 g) was added dropwise over a period of 2 hours. After stirring for another 1 hour, amidosulphuric acid (2.5 g, 0.026 mol) was added. Copper(I) chloride (10.8 g, 0.11 mol), hydrochloric acid (202 g, 31%, 1.72 mol) and water (75 g) were placed in a second flask and the diazonium salt generated previously was added dropwise over a period of 30 minutes. After stirring for another 1.5 hours, the mixture was extracted with dichloromethane (250 g), the phases were separated and dichloromethane was distilled off under reduced pressure. The crude product obtained was purified by distillation. 2-Bromo-4-chloro-1-isopropylbenzene (62.6 g, 94.8 GC-% by area. 59% of theory) was obtained as a colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440908B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-75e5646be5c9480fba177cf39bd72a36
Quellennotizuspto-grants-2016_09