HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292635Generated: November 2, 2026
Pyridine → Ethyl 3-(4-carboxy-2-methylphenylhydrazono)-4-oxopentanoate
https://huagongshe.com/reaction/2292635
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Amino-3-methylbenzoic acid | HCID 75598 | — |
| Reactant | Ethyl 3-acetyl-4-oxopentanoate | HCID 87820 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-(4-carboxy-2-methylphenylhydrazono)-4-oxopentanoate | HCID 86751496 | — |
Reaction Steps
A mixture of 3 g (19.8 mmol) of 4-amino-3-methylbenzoic acid in 50 ml of water and 50 ml of ethanol and 3.56 ml of concentrated hydrochloric acid was cooled in an ice bath and then 1.5 g of NaNO2 (21.8 mmol) in 10 ml of water was added portionwise. The mixture was allowed to come to room temperature and then added to a solution of 4.06 g (21.8 mmol) of ethyl 3-acetyl-4-oxopentanoate and 8 ml of pyridine in 25 ml of ethanol. The reaction mixture was left for 24 hr at room temperature with stirring. The mixture was acidified with concentrated hydrochloric acid and the mixture diluted with 20 ml of water. The resulting solid was collected and washed with water and pentane to yield 5.2 g of ethyl 3-(4-carboxy-2-methylphenylhydrazono)-4-oxopentanoate with m.p. 161°-162.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05684024 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-c00576b04f1c4997b885d644cc60d1bd |
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| Source note | uspto-grants-1997_11 |
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