HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761548Generated: November 1, 2026
Ethyl 2-chloroacetoacetate → HCID 14500704, compound
https://huagongshe.com/reaction/1761548
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2-chloroacetoacetate | HCID 11858 | — |
| Reactant | N-(2-Phenylethyl)hydrazinecarbothioamide | HCID 2305793 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14500704 | HCID 14500704 | — |
Reaction Steps
A stirred slurry of 33.1 g (0.17 mole) of 4-phenylethyl-3-thiosemicarbazide in 500 mL of absolute ethanol under nitrogen atmosphere was treated with 29 g (0.17 mole) of ethyl 2-chloroacetoacetate, stirred at ambient temperature for ~72 hr, heated to reflux to dissolve most materials, and filtered hot. The filtrate was concentrated in vacuo to give a reddish oil, 71 g. The residue was chromatographed on 800 g Florosil® and eluted first with benzene to remove a yellow band (sulfur) followed by an acetone/benzene gradient which gave two main fractions. These two fractions were combined, and concentrated to give a yellow oil which solidified. Recrystallization (twice) from ligroin gave a fluffy white crystalline product, with small spots of green-yellow color, 12.1 g, mp 138°-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04826866 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-226e17577cfd46329a94bdd85f832c7e |
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| Source note | uspto-grants-1989_05 |
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