Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 262435Erstellt: 26. Oktober 2026

Ethylene Glycol → 6,7-Dimethyl-naphthalene-1,4-dicarboxylic acid

https://huagongshe.com/reaction/262435

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktGlyoxalHCID 7860—
EduktPotassium HydroxideHCID 14797—
Edukt2-[2-(Cyanomethyl)-4,5-dimethylphenyl]acetonitrileHCID 305142—
EduktGlyoxal hydrateHCID 21880647—
LösungsmittelMethanolHCID 887—
Produkt6,7-Dimethyl-naphthalene-1,4-dicarboxylic acidHCID 2029407831%

Reaktionsschritte

18.4 parts of 4,5-dimethyl-1,2-bis-cyanomethyl-benzene and 8.4 parts of glyoxal hydrate (trimer) (3C2H2O2.2H2O), containing 80% of glyoxal to be liberated, are stirred in 100 parts by volume of methanol. With stirring and under nitrogen, 11.2 parts of powdered potassium hydroxide are added to the reaction mixture by small amounts at 0° to 5° C. After the addition of potassium hydroxide, stirring is continued for 5 hours at 0° to 5° C. under nitrogen. The slightly brown coloured reaction mixture is subsequently diluted with 100 parts by volume of ethylene glycol and then, after addition of 28 parts of potassium hydroxide, heated slowly to 190° C. under nitrogen while the methanol is distilled off and ammonia escapes at 80° C. After it has been stirred for 5 hours at 185° to 190° C. under nitrogen, the reaction mixture is worked up as described in Example 7 to yield 7.5 parts of 6,7-dimethyl-naphthalene-1,4-dicarboxylic acid (31% of theory) of formula ##STR52## in the form of slightly brown crystalline powder with a melting point of 268°-280° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04154754
Quelldatensatzuspto-grants-1979_05
ORD IDord-30065f9e5db74ae8a3ea7f20249c7df4
Quellennotizuspto-grants-1979_05