HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260655Generated: November 1, 2026
4-tert-Butylphenol → HCID 18998871, compound
https://huagongshe.com/reaction/2260655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 18998870 | HCID 18998870 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18998871 | HCID 18998871 | 72.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05478849 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-bdec988b07454d708b26e974398ec4aa |
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| Source note | uspto-grants-1995_12 |
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