HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50031Generated: October 26, 2026
Hydrochloric Acid → Ethyl Pyruvate 4-Chloro-3-Fluorophenylhydrazone
https://huagongshe.com/reaction/50031
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 2-methylacetoacetate | HCID 701 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 4-Chloro-3-fluoroaniline | HCID 2736511 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl Pyruvate 4-Chloro-3-Fluorophenylhydrazone | HCID 73115740 | 30.3% |
Reaction Steps
A solution of sodium nitrite (4.76 g, 0.069 mol) in water (6.3 mL) was added dropwise to an ice cooled mixture of 4-chloro-3-fluoroaniline (J. Am. Chem. Soc., 1996, 61, 5130-5133) (10.00 g, 0.069 mol), water (167 mL) and 37% hydrochloric acid (167 mL). After 20 minutes potassium acetate (9.81 g, 0.10 mol) was added, and then a solution of ethyl 2-methylacetoacetate (9.95 g, 0.069 mol), potassium acetate (9.81 g, 0.10 mol) in methanol (67 mL) was dropped while cooling on the ice bad. Reaction was stirred at 0° C. for 3 hours, then extracted with diethyl ether. Organic layer was washed with brine and dried. Removal of the solvent furnished a red oily residue that was treated with ethanol (100 mL) and stirred at room temperature overnight. The solid which formed was filtered a recrystallized from ethanol to give 5.4 g (30%) of title compound, mp 161-163° C. (from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06710068B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-fd12142649ea4bb5af36be8b36b06f39 |
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| Source note | uspto-grants-2004_03 |
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