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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Monoethyl succinate | HCID 70610 | — |
| Reactant | 2-Chloroethyl formate | HCID 246748 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 4-[2-(aminocarbothioyl)hydrazino]-4-oxobutanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07241785B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-b473733af0944ed5aa429a4bc0f0f3c7 |
|---|
| Source note | uspto-grants-2007_07 |
|---|