HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606445Generated: October 30, 2026
Ethyl 3-chloro-3-oxopropionate → Ethyl 3-[2-(aminocarbonothioyl)hydrazino]-3-oxopropanoate
https://huagongshe.com/reaction/606445
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 3-chloro-3-oxopropionate | HCID 118931 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl 3-[2-(aminocarbonothioyl)hydrazino]-3-oxopropanoate | HCID 57708832 | 42% |
Reaction Steps
To a suspension of hydrazinecarbothioamide (15.0 g, 165 mmol) in pyridine (100 mL) was added dropwise ethyl 3-chloro-3-oxopropanoate (24.8 g, 165 mmol) over 30 min at 0° C., and the reaction solution was stirred at room temperature for 2 days. The reaction mixture was concentrated under reduced pressure, and methanol was added to the residue. The resulting solid was filtered off, the filtrate was concentrated under reduced pressure, and the residue was extracted with ethyl acetate, THF and saturated aqueous ammonium chloride solution. The organic layer was washed with saturated aqueous ammonium chloride solution, dried over sodium sulfate, and concentrated. The residue was crystallized from ethyl acetate and isopropyl ether, and the obtained crystals were washed with isopropyl ether, and dried to give the title compound (14.2 g, 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915267B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-b155e76596ae45869a8204f9deba5725 |
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| Source note | uspto-grants-2011_03 |
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