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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651157Generated: November 2, 2026

Triethylamine → HCID 54570443, compound

https://huagongshe.com/reaction/1651157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
ReactantHCID 86743945HCID 86743945—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 54570443HCID 5457044364%

Reaction Steps

To a solution of 2-cyano-2-(1-ethoxycarbonyl-1-methylethoxyimino)acetamidine acetate (685 g) in methanol (6.85 l) was added triethylamine (557 g) at -13~-15° C. over a 20-minute period and then bromine (344 g) was added thereto at the same temperature over the same period. The solution was stirred at -13~-15° C. for 15 minutes, then N,N-dimethylformamide (685 ml) was added to the solution at the same temperature, and a solution of potassium thiocyanate (209 g) in methanol (2.09 l) was added thereto at -13~-15° C. over a 30-minute period. After being stirred at -5 ~0° C. for an hour, the solution was poured into a cold water (5 ~10° C.) and stirred for an hour under ice-cooling. The resulting precipitates were collected by filtration, washed with cold water and dried to give 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(l-ethoxycarbonyl-1-methylethoxyimino)acetonitrile (390 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927818
Source datasetuspto-grants-1990_05
ORD IDord-f48c6be3a9a649bfb145839f58aeeb05
Source noteuspto-grants-1990_05