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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414513Generated: October 27, 2026

Benzenediazonium chloride → 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid

https://huagongshe.com/reaction/414513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenediazonium chlorideHCID 60992—
ReactantSodiumHCID 5360545—
Reactant3-Hydroxy-5-oxocyclohex-3-ene-1-carboxylic acidHCID 14492370—
SolventMethanolHCID 887—
Product3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acidHCID 135583503—

Reaction Steps

13.8 g. of sodium were dissolved in 900 ml. of methanol and to this solution were added 46.8 g. of 3-hydroxy-5-keto-3-cyclohexene-carboxylic acid. The resulting mixture was stirred, maintained between -4° C. and -8° C. by means of a cooling bath and treated over a period of 30 minutes with a phenyl-diazonium chloride solution (prepared from 27.9 g. of aniline, 450 ml. of water, 72 ml. of concentrated hydrochloric acid and 21.0 g. of sodium nitrite in 90 ml. of water). The resulting mixture was stirred for an additional hour at -5° C. to -10° C. The precipitated red reaction product was removed by filtration with suction and washed with about 1000 ml. of water, whereby there was obtained 3-hydroxy-5-keto-4-phenylazo-3-cyclohexene-carboxylic acid having a melting point of 218° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792557
Source datasetuspto-grants-1988_12
ORD IDord-01d273bae5c54d28958c140aca35855d
Source noteuspto-grants-1988_12