Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Reactant | 2,6-Dimethylphenyl carbonochloridate | HCID 271618 | — |
| Product | 2-Fluoro-m-xylene | HCID 123065 | 58.3% |
Reaction Steps
1.1 kg of anhydrous hydrogen fluoride were placed in a 3 l autoclave and the autoclave was sealed and heated to 130° C. At this temperature, 1 kg of 2,6-dimethylphenyl chloroformate was pumped in over a period of 3 hours, the pressure of the gases formed being released at 40 bar. Finally, the mixture was stirred for 1 hour at 130° C. The reaction mixture was then cooled and excess hydrogen fluoride was distilled off at 100 mbar. Further working-up of the reaction mixture was carried out as described in Example 9. 2,6-Dimethylfluorobenzene was obtained in a yield of 58.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05306849 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-685a5566410848a4ac1a06d910f32a26 |
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| Source note | uspto-grants-1994_04 |
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