HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072024Generated: October 26, 2026
Phenol → (2,2-Dichloro-1,1-difluoroethoxy)benzene
https://huagongshe.com/reaction/2072024
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 1,1-Dichloro-2,2-difluoroethene | HCID 6592 | — |
| Reactant | Dichlorodifluoroethene | HCID 11736 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (2,2-Dichloro-1,1-difluoroethoxy)benzene | HCID 13529258 | — |
Reaction Steps
In a 500 ml stirred reaction flask equipped with thermometer, air condenser, dropping funnel and ice water bath was placed 94 g (one mole) of phenol and 300 ml of acetone and the mixture was cooled to 10° C. 11.0 Grams of powdered KOH (85 percent) was then added. After the mixture was stirred for one-half hour at 10° C., 2,2-dichloro-1,1-difluoroethene was introduced over a period of one hour while maintaining the temperature at about 10-12° C. At the end of the addition of the dichlorodifluoroethene, a rapid reaction increased the temperature to 50° C. A Dry Ice(R) bath was substituted for the ice bath to cool the reaction mixture to 10° C. rapidly. After stirring overnight, the reaction mixture was poured over two liters of ice, stirred, allowed to settle and the oil layer was separated. The oil layer was washed with bicarbonate of soda solution and with water and the nearly colorless organic layer was separated. After drying over desiccant-grade magnesium sulfate, the organic layer was filtered to give the first-step product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04049693 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-73166a90e0804d4c88d5c1f7e46f0f0f |
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| Source note | uspto-grants-1977_09 |
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