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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPotassium HydroxideHCID 14797—
ReactantN,N-Diethyl-2-hydroxyacetamideHCID 4137580—
Reactant5-Chloro-3-(trifluoromethyl)-1,2,4-thiadiazoleHCID 13279589—
SolventWaterHCID 962—
Product(3-Trifluoromethyl-1,2,4-thiadiazol-5-yl)-oxyacetic acid diethylamideHCID 1327959347.1%

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04549899
Source datasetuspto-grants-1985_10
ORD IDord-21355d72c54840299639fa86057640b6
Source noteuspto-grants-1985_10