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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033183Generated: November 1, 2026

Tetrabutylammonium Fluoride → HCID 19025402, compound

https://huagongshe.com/reaction/1033183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 19025422HCID 19025422—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19025402HCID 1902540270.7%

Reaction Steps

To a stirred mixture of 4.40 g (0.0119 mole) of 3-trifluoromethyl-4,5-dihydro-1-methyl -4-(2-methyl-4-trimethylsilylethynylphenyl)-1,2,4-triazol-5-(1H)-thione in 75 ml of tetrahydrofuran was added 10.8 g (0.0414 mole) of tetrabutylammonium fluoride. This mixture was stirred for about 20 minutes, and the reaction was partitioned between 75 ml of diethyl ether and 150 ml of an aqueous sodium chloride solution. The organic phase was dried over anhydrous magnesium sulfate and was filtered. The filtrate was evaporated under reduced pressure, leaving a residue. This residue was purified by column chromatography on silica gel, eluting with diethyl ether, to yield 2.5 g of 4-(4-ethynyl-2-methylphenyl)-3-trifluoromethyl-4,5-dihydro-1-methyl-1,2,4-triazol-5(1H)-thione as an oil, Compound 111 of Table 1. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310724
Source datasetuspto-grants-1994_05
ORD IDord-c68ccf650f6a4d9392014d8b4ab799b7
Source noteuspto-grants-1994_05