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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660325Generated: November 2, 2026

Ethoxalyl chloride → 1-Ethyl-1-ethoxalyl-thiosemicarbazide

https://huagongshe.com/reaction/1660325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxalyl chlorideHCID 20884—
Reactant2-EthylhydrazinecarbothioamideHCID 22105028—
SolventAcetoneHCID 180—
Product1-Ethyl-1-ethoxalyl-thiosemicarbazideHCID 20558125—

Reaction Steps

Ethoxalyl chloride (10.6 cc) is added dropwise, in the course of 10 minutes, to a solution, at 20° C., of 1-ethyl-thiosemicarbazide (11.9 g) in acetone (200 cc). The temperature rises to 43° C., the mixture is stirred for 1 hour without heating and is concentrated to dryness at 20° C. under 20 mm Hg (2.7 kPa), the residue is taken up in methanol (30 cc) and the crystallisation is started. After filtration and drying, 1-ethyl-1-ethoxalyl-thiosemicarbazide (13.2 g) is obtained in the form of a white solid melting at 170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307116
Source datasetuspto-grants-1981_12
ORD IDord-c40b265242454c35a03a82b06c881f90
Source noteuspto-grants-1981_12