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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-chloro-3-oxopropionateHCID 118931—
ReactantThiosemicarbazideHCID 2723789—
SolventPyridineHCID 1049—
ProductEthyl 3-[2-(aminocarbonothioyl)hydrazino]-3-oxopropanoateHCID 5770883242%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915267B2
Source datasetuspto-grants-2011_03
ORD IDord-b155e76596ae45869a8204f9deba5725
Source noteuspto-grants-2011_03