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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 5-[1-(4-Chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-amine | HCID 3155972 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-[1-(4-Chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-yl isocyanate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04264353 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-d5ce8d4525664a9aa45bb750c5a26806 |
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| Source note | uspto-grants-1981_04 |
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