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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenediazonium chloride | HCID 60992 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 3-Hydroxy-5-oxocyclohex-3-ene-1-carboxylic acid | HCID 14492370 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04792557 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-01d273bae5c54d28958c140aca35855d |
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| Source note | uspto-grants-1988_12 |
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