HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391074Generated: October 25, 2026
Carbon Tetrachloride → alpha,alpha'-Dichloro-2,5-difluoro-para-xylene
https://huagongshe.com/reaction/1391074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 1,4-Benzenedimethanol, 2,5-difluoro- | HCID 22630192 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | alpha,alpha'-Dichloro-2,5-difluoro-para-xylene | HCID 21332303 | — |
Reaction Steps
While cooling with ice, 3 g of triethylamine are added to a mixture of 25 g of phosphorus pentachloride and 25 g of phosphorus oxychloride. After that, a solution of 2.2 g of α,α'-dihydroxy-2,5-difluoro-para-xylene in 10 ml of tetrachloromethane are added. The batch is heated at 70° C. for two hours. It is then cooled, poured onto ice, and dissolved in benzene. The benzene solution is washed with aqueous sodium carbonate solution, then dried with calcium chloride. The solvent is evaporated and the residue recrystallized several times from aqueous methanol. There are obtained 1.85 g of fine colorless needles melting at 62.5 - 64.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04140843 |
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| Source dataset | uspto-grants-1979_02 |
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| ORD ID | ord-6a17fcba63804977894d0c2c861704a7 |
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| Source note | uspto-grants-1979_02 |
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