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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616874Generated: October 31, 2026

Hydrochloric Acid → 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid

https://huagongshe.com/reaction/616874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnilineHCID 6115—
ReactantBenzenediazonium chlorideHCID 60992—
ReactantSodiumHCID 5360545—
Reactant3-Hydroxy-5-oxocyclohex-3-ene-1-carboxylic acidHCID 14492370—
ReactantSodium NitriteHCID 23668193—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acidHCID 135583503—

Reaction Steps

13.8 G. of sodium were dissolved in 900 ml. of methanol. 46.8 G. of 3-hydroxy-5-keto-3-cyclohexenecarboxylic acid were added to this solution. The mixture was stirred, maintained between -4° C. and -8° C. with 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 mixture was stirred -5° C. to -10° C. for an additional hour. The resulting red precipitate was removed by filtration under vacuum and washed with about 1000 ml. of water, thereby there was obtained 3-hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid of melting point 218° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04076810
Source datasetuspto-grants-1978_02
ORD IDord-d1a9d283acfb44b9bc43ae8e25b18890
Source noteuspto-grants-1978_02