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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1018176Erstellt: 26. Oktober 2026

Ammonia → 4-Amino-3,5-dichlorobenzotrifluoride

https://huagongshe.com/reaction/1018176

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktLithium fluorideHCID 224478—
Edukt1,2,3-Trichloro-5-(trifluoromethyl)benzeneHCID 2733399—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt4-Amino-3,5-dichlorobenzotrifluorideHCID 14109472,2%

Reaktionsbedingungen

Temperatur-95 °C

Reaktionsschritte

3,4,5-Trichloro-trifluoromethylbenzene (0.681 g, 2.73 mmol), lithium fluoride (7.1 mg, 0.273 mmol) and N-methylpyrrolidone (1.8 ml) are mixed in an autoclave. The autoclave is cooled to −95° C. and then ammonia (1.3 g, 76.4 mmol) is added. The autoclave is then heated at 250° C. and with stirring for 4 h and is subsequently allowed to return to room temperature. The reaction product is extracted by washing with water and with dichloromethane and then the organic phase is evaporated, after having been dried. 0.453 g (1.97 mmol) of 2,6-dichloro-4-trifluoromethylaniline is obtained with a degree of conversion of the 3,4,5-trichloro-trifluoromethylbenzene of 97%, a ratio equal to 83/17 for the selectivity for 2,6-dlchloro-para-trifluoromethylaniline with respect to 2,6-dichloro-meta-trifluoromethylaniline and an 87% yield of 2,6-dichloro-para-trifluoromethylaniline.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06479703B1
Quelldatensatzuspto-grants-2002_11
ORD IDord-6475831cd98b4b2986b7ef106e72a8e5
Quellennotizuspto-grants-2002_11