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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379582Generated: November 2, 2026

Acetic Acid → HCID 178481700, compound

https://huagongshe.com/reaction/1379582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanto-(Trifluoromethyl)benzaldehydeHCID 123067—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178527894HCID 178527894—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 178481700HCID 178481700—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2.0 g of 3-mercapto-1,2,4-triazole in 80 ml THF at -78° C., 14.0 ml of a 2.5M solution of n-butyl lithium in hexane were added over a period of 10 minutes. The color of the reaction mixture changed to creamy yellow, then to white, half-way through the addition. Stirring was continued at -78° C. for 1 hour and then the temperature was allowed to rise to 0° C. and kept there for one hour. The reaction mixture was cooled again to -78° C. and 1.6 g of 2-trifluoromethylbenzaldehyde were added slowly. The color of the reaction mixture changed to yellow. The reaction mixture was allowed to warm to room temperature and stirred overnight. The resulting orange solution was cooled to 0° C. and about 1 ml of glacial acetic acid was added. A yellow precipitate formed, which was removed by filtration and put onto a silica gel column. Elution with hexane, then a 1:1 mixture of hexane and diethyl ether, and then diethyl ether yielded 1.1 g of 3-(1-hydroxy-2'-trifluoromethylbenzyl)-4-methyl-5-mercapto-1,2,4-triazole in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05672567
Source datasetuspto-grants-1997_09
ORD IDord-78ecb28cab1344679f08c7ba7e52d05f
Source noteuspto-grants-1997_09