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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260655Generated: November 1, 2026

4-tert-Butylphenol → HCID 18998871, compound

https://huagongshe.com/reaction/2260655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylphenolHCID 7393—
ReactantSodium hydrideHCID 24758—
ReactantHCID 18998870HCID 18998870—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 18998871HCID 1899887172.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension formed by suspending 0.16 g of sodium hydride (60%) in N,N-dimethylformamide was added 0.6 g of 4-t-butylphenol and after stirring the mixture for one hour at 60° C., 0.81 g of 3-(4-t-butylphenoxy)-4-chloro-1,2,5-thiadiazole was added to the mixture followed by stirring for 12 hours at 100° C. After allowing to cool, the reaction mixture was poured in water and extracted with ether. The ether layer collected was washed twice each time with a diluted aqueous sodium hydroxide solution, water, and then a saturated aqueous sodium chloride solution. The ether layer thus washed was dried with anhydrous magnesium sulfate, concentrated, and purified by silica column chromatography to provide 0.84 g of 3,4-bis(4-t-butylphenoxy)-1,2,5-thiadiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478849
Source datasetuspto-grants-1995_12
ORD IDord-bdec988b07454d708b26e974398ec4aa
Source noteuspto-grants-1995_12