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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2052276Erstellt: 25. Oktober 2026

Nitrobenzene → HCID 20377537, Verbindung

https://huagongshe.com/reaction/2052276

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrobenzeneHCID 7416—
Edukt2-Chloro-5-fluoroanisoleHCID 2724520—
EduktAluminum(III) ChlorideHCID 6451240—
EduktHCID 22632797HCID 22632797—
ProduktHCID 20377537HCID 20377537—

Reaktionsschritte

Under ice-cooling, monoethyl oxalate monochloride (10.5 g) is added dropwise to a solution of aluminum chloride (10.5 g) in nitrobenzene (30 ml). To the solution is added dropwise 2-chloro-5-fluoroanisole (84 g). After 30 minutes, the mixture is poured into ice-water and extracted with ether. The extract is washed with dilute hydrochloric acid and dilute aqueous sodium bicarbonate, dried and evaporated to remove the solvent. Recrystallization from a mixture of ether and n-hexane gives ethyl 4-methyl-3-chloro-6-fluorophenylglyoxalate (mp. 84°-85° C.). A mixture of the glyoxalate (5.21 g), ethylene glycol (28 ml), potassium hydroxide (4.5 g) and hydrazine monohydrate (2.85 ml) is heated at 155°-158° C. for 1.5 hours and then at 220° C. for 2 hours and poured into water. The mixture is washed with ether, acidified with hydrochloric acid and extracted with ether. The extract is evaporated. The obtained residue is recrystallized from dichloromethane to give 3-chloro-4-hydroxy-6-fluorophenylacetic acid (mp. 137°-138° C.). A part of the acid (0.615 g) is suspended in dichloromethane (15 m) and esterified with diphenyldiazomethane to give crystals of the corresponding diphenylmethyl ester (mp. 121°-122° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04183928
Quelldatensatzuspto-grants-1980_01
ORD IDord-5d0fd0e274c142fdadcb09382d5b9889
Quellennotizuspto-grants-1980_01