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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444369Generated: October 31, 2026

Phosgene → 5-[1-(4-Chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-yl isocyanate

https://huagongshe.com/reaction/444369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
Reactant5-[1-(4-Chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-amineHCID 3155972—
SolventEthyl AcetateHCID 8857—
Product5-[1-(4-Chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-yl isocyanateHCID 13020764—

Reaction Steps

A 500 millileter, 3-neck flask equipped with a magnetic stirrer, thermometer, dry ice condensor/drying tube and inlet from a phosgene (COCl2) tank via a calibrated rotometer was charged with 50 milliliters of ethylacetate saturated with phosgene at 20° C. (approximately 0.5 mole of phosgene). Additional 100 ml. of ethylacetate was added; (8.9 grams of 5-[1-(4-chlorophenoxy) ethyl]-2-amino-1,3,4-thiadiazole, (prepared above) at a temperature from 0° C. to room temperature was added. The resulting solution was stirred for 17 hours with formation of an emulsion, and then the flask was purged with nitrogen until no COCl2 was detected. The solution was filtered through a Whatman #42 filter paper to yield a slightly cloudy solution which was topped at 60 degrees centigrade with a roto-vac to form 9.2 grams of a pale yellow goop of 5-[1-(4-chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-yl isocyanate dimer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264353
Source datasetuspto-grants-1981_04
ORD IDord-d5ce8d4525664a9aa45bb750c5a26806
Source noteuspto-grants-1981_04