HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464911Generated: October 31, 2026
Isopropanol → (3-Trifluoromethyl-1,2,4-thiadiazol-5-yl)-oxyacetic acid diethylamide
https://huagongshe.com/reaction/464911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N,N-Diethyl-2-hydroxyacetamide | HCID 4137580 | — |
| Reactant | 5-Chloro-3-(trifluoromethyl)-1,2,4-thiadiazole | HCID 13279589 | — |
| Solvent | Water | HCID 962 | — |
| Product | (3-Trifluoromethyl-1,2,4-thiadiazol-5-yl)-oxyacetic acid diethylamide | HCID 13279593 | 47.1% |
Reaction Steps
5.6 g (0.03 mol) of 5-chloro-3-trifluoromethyl-1,2,4-thiadiazole are added to a mixture which comprises 4 g (0.03 mol) of hydroxyacetic acid diethylamide, 1.9 g (0.03 mol) of potassium hydroxide powder and 80 ml of isopropanol and has been cooled to -10° C. The reaction mixture is stirred for 10 hours at -10° C. and poured into water, and the product is filtered off under suction. 4 g (47% of theory) of (3-trifluoromethyl-1,2,4-thiadiazol-5-yl)-oxyacetic acid diethylamide are obtained in the form of white crystals of melting point 60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04549899 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-21355d72c54840299639fa86057640b6 |
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| Source note | uspto-grants-1985_10 |
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