Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Reactant | 2,6-Dimethylphenyl carbonochloridate | HCID 271618 | — |
| Product | 2-Fluoro-m-xylene | HCID 123065 | — |
| Product | 2,6-Dimethylphenylfluoroformate | HCID 10844827 | — |
Reaction Steps
500 ml of anhydrous hydrogen fluoride were placed at 0° C. in a stainless steel laboratory autoclave and 1000 g of 2,6-dimethylphenyl chloroformate were added dropwise. The autoclave was then sealed and heated at a maximum temperature of 110° C. for 2 hours, the pressure of the gases formed being released at 30 bar. The reaction mixture was worked up as described in Example 9. Distillation gave 2,6-dimethylfluorobenzene in a yield of 11% and 2,6-dimethylphenyl fluoroformate in a yield of 68%. The latter can be added to a new batch for the preparation of 2,6-dimethylfluorobenzene (see Example 15).
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-f4d44997ea8549468350defcded2853f |
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| Source note | uspto-grants-1994_04 |
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