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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262435Generated: October 25, 2026

Ethylene Glycol → HCID 20294078, compound

https://huagongshe.com/reaction/262435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantGlyoxalHCID 7860—
ReactantPotassium HydroxideHCID 14797—
Reactant2-[2-(Cyanomethyl)-4,5-dimethylphenyl]acetonitrileHCID 305142—
ReactantGlyoxal hydrateHCID 21880647—
SolventMethanolHCID 887—
ProductHCID 20294078HCID 2029407831%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154754
Source datasetuspto-grants-1979_05
ORD IDord-30065f9e5db74ae8a3ea7f20249c7df4
Source noteuspto-grants-1979_05