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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295265Generated: October 26, 2026

Hydrochloric Acid → Ethyl 4-[2-(aminocarbothioyl)hydrazino]-4-oxobutanoate

https://huagongshe.com/reaction/1295265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMonoethyl succinateHCID 70610—
Reactant2-Chloroethyl formateHCID 246748—
ReactantThiosemicarbazideHCID 2723789—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductEthyl 4-[2-(aminocarbothioyl)hydrazino]-4-oxobutanoateHCID 22930781—

Reaction Steps

To a solution of succinic acid monoethyl ester (22.0 g) and triethylamine (16.8 g) in tetrahydrofuran (150 ml) was added dropwise chloroethyl formate (18.0 g) at −20° C. After stirring for 30 min., pulverized thiosemicarbazide (13.7 g) was added and the mixture was stirred at room temperature for 7 hrs. Water was added to the reaction mixture, acidified with 2N hydrochloric acid and extracted with chloroform. The aqueous layer was separated and sodium chloride was added. The mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residual crystals were recrystallized from dichloromethane-ethanol to give ethyl 4-[2-(aminocarbothioyl)hydrazino]-4-oxobutanoate as colorless prism crystals (8.23 g, 25%). melting point: 143–144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-b473733af0944ed5aa429a4bc0f0f3c7
Source noteuspto-grants-2007_07