HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090179Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 19914734, compound
https://huagongshe.com/reaction/1090179
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | HCID 19914729 | HCID 19914729 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19914734 | HCID 19914734 | — |
Reaction Steps
An amount of 6.1 of potassium tert-butoxide is added, under nitrogen atmosphere at -10° C., to 1.9 g of 2-(4-chlorphenyl)-2-methyl-3-(1,2,4-triazol-1-yl)-1-hydroxy-propane dissolved in 6.5 ml of anhydrous THF, 13 ml. of anhydrous DMSO, and 13 ml of anhydrous tert. butanol. The apparatus is then first put under vacuum and tetrafluoroethylene is introduced by maintaining the reaction mass under this gas atmosphere over a time of one night, at room temperature. The reaction mixture then is poured into water, and extracted with ethyl acetate. The extract is washed with water, dried over Na2SO4 and evaporated; the raw product obtained is purified by chromatography over silica gel, using n-hexane-ethyl acetate 1:1 as eluent. 1 g of an oil is isolated having the structure indicated in the title of this example, according to the following spectroscopic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05081141 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-99b1ac773fc94a92978a73b9ebb8f241 |
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| Source note | uspto-grants-1992_01 |
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