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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 749261Erstellt: 24. Oktober 2026

Methane → (2-Chloro-6-fluorophenyl)-P-tolyl-amine

https://huagongshe.com/de/reaction/749261

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
EduktHydrochloric AcidHCID 313—
Eduktp-ToluidineHCID 7813—
EduktBinap, (A+-)-HCID 634876—
Edukt2-Bromo-1-chloro-3-fluorobenzeneHCID 21938660—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt(2-Chloro-6-fluorophenyl)-P-tolyl-amineHCID 21100364103,2%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 2-bromo-1-chloro-3-fluorobenzene (32 g, 153 mmol), p-toluidine (16.4 g, 153 mmol), sodium tert.butylate (27.5 g, 286 mmol), (±)-BINAP [2,2′-Bis-(diphenylphosphino)-1,1′-binaphthalin, 0.66 g, 1.1 mmol) and toluene (250 ml) is stirred under nitrogen for about 30 minutes. After the addition of Palladium-bis-(dibenzylidenaceton) (0.8 g, 1 mmol), the mixture is heated to 110° C. (slight reflux) for 14-20 hours. The mixture is then cooled to 30° C., water (60 ml), concentrated hydrochloric acid (60 ml) as well as charcoal and cellite (5 g each) are added and stirring is continued for an hour. The mixture is filtered and the filtrate is separated into the phases. The organic phase is washed with water (3 times, 70 ml each) and concentrated in vacuo to obtain 37.2 g of crude (2′-chloro-6′-fluorophenyl)-(4-methylphenyl)-amine. The product can be used in the next step (Step 1.2) as such; alternatively in can be kugelrohrdistilled in vacuo.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07402603B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-3628d3297d5b49e9ac3bfa4c1c247357
Quellennotizuspto-grants-2008_07