HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735367Generated: October 29, 2026
Chlorodifluoromethane → 4-Difluoromethoxy-4'-octoxy-biphenyl
https://huagongshe.com/reaction/1735367
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Hydroxy-4'-octyloxybiphenyl | HCID 10494329 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Difluoromethoxy-4'-octoxy-biphenyl | HCID 14765968 | — |
Reaction Steps
A mixture of 20 g of 4-hydroxy-4'-octyloxybiphenyl, 13.6 g of NaOH, 100 ml of water and 150 ml of dioxane is heated to 70° C. with stirring. 10 g of chlorodifluoromethane are passed into the cooled two-phase mixture with vigorous stirring. The reaction mixture is poured into water, and the product is extracted with petroleum ether. The organic phase is dried over Na2SO4, evaporated, and the residue is filtered through a short silica gel column using petroleum ether as eluent. The product is recrystallized from acetonitrile. Colorless crystals are obtained. m.p.: 104° C., c.p.: 20° C. (extrapolated), Δn=0.093, viscosity: 17.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05536442 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-d3d435b03dd6489b8ac55b178252007c |
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| Source note | uspto-grants-1996_07 |
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