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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052252Generated: October 31, 2026

Trifluoroacetic acid → HCID 178513859, compound

https://huagongshe.com/reaction/2052252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantHCID 178490897HCID 178490897—
ProductHCID 178513859HCID 17851385999.1%

Reaction Steps

3-Carbamoyl-4-(p-methoxybenzyl)-1,2,4-triazole-5-thiol (2.0 g., 0.007 mole), trifluoroacetic acid (8 ml.) and anisole (2 ml.) were heated at 70° C. for 3.5 hours. At this point, most of the trifluoroacetic acid present was removed by means of evaporation under reduced pressure and the residue was subsequently triturated with diethyl ether. The resulting solid was then filtered, washed with diethyl ether and subsequently dried in vacuo at 50° C. to give pure 3-carbamoyl-1,2,4-triazole-5-thiol (1.0 g., 91% yield), m.p. 276°-278° C. The infrared absorption spectrum was identical to that of a reference sample prepared as described in Example XVI, Part C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04183925
Source datasetuspto-grants-1980_01
ORD IDord-91b4a7fbe00f42d0807d9117388945a8
Source noteuspto-grants-1980_01