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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833805Generated: November 1, 2026

Chloroacetyl isocyanate → N-(Chloroacetyl)-5-ethoxy-3-oxo-1,2,4-thiadiazole-2(3H)-carboxamide

https://huagongshe.com/reaction/1833805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl isocyanateHCID 78209—
ReactantHCID 178467476HCID 178467476—
SolventBenzeneHCID 241—
ProductN-(Chloroacetyl)-5-ethoxy-3-oxo-1,2,4-thiadiazole-2(3H)-carboxamideHCID 2138750958%

Reaction Conditions

Temperature20 °C

Reaction Steps

31.5 g of α-chloroacetyl isocyanate were added dropwise to a solution of 18.98 g of 3-hydroxy-5-ethoxy-1,2,4-thiadiazole in 200 ml of benzene and after stirring the mixture for 17 hours at 20° C, it was vacuum filtered. The recovered crystals were dried to obtain 20 g of 2-(N-α-chloroacetylcarbamoyl)-5-ethoxy-1,2,4-thiadiazole-3-one melting at 132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04067720
Source datasetuspto-grants-1978_01
ORD IDord-abec7180f484464fbcf5172e68d0501e
Source noteuspto-grants-1978_01