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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127140Generated: October 30, 2026

Oxalyl chloride → 5-[N-(1-ethylpropyl)aminosulfonyl]-1,3,4-thiadiazol-2-yl isocyanate

https://huagongshe.com/reaction/127140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-amino-5-[N-(1-ethylpropyl)aminosulfonyl]-1,3,4-thiadiazoleHCID 20286109—
SolventO-XyleneHCID 7237—
Product5-[N-(1-ethylpropyl)aminosulfonyl]-1,3,4-thiadiazol-2-yl isocyanateHCID 54446009—

Reaction Steps

2-Amino-5-[N-(1-ethylpropyl)aminosulfonyl]-1,3,4-thiadiazole (0.10 mole) and xylene (200 ml) are charged into a glass reaction vessel fitted with a mechanical stirrer, thermometer and condenser. The mixture is dried by azeotroping off water and is then cooled to room temperature. Oxalyl chloride (0.15 mole) is added; the reaction mixture is warmed to a temperature of from 80° C. to about 100° C. and stirred at this temperature for a period of about 1 hour. The mixture is then heated to reflux and stirred for an additional 2 hours. Solvent is then stripped off leaving the desired product 5-[N-(1-ethylpropyl)aminosulfonyl]-1,3,4-thiadiazol-2-yl isocyanate dimer as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255182
Source datasetuspto-grants-1981_03
ORD IDord-84b057d066fd4023813f0b2a8a1a621f
Source noteuspto-grants-1981_03