Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorophenol | HCID 4684 | — |
| Reactant | HCID 19810908 | HCID 19810908 | — |
| Product | 4-Chloro-2-fluorophenol | HCID 181975 | 69% |
Reaction Steps
The procedure of a) was used except that 0.64 g of 4-chlorophenol was employed, the fluorinating agent was 1.89 g of N-fluoro-2,3-dichloro-6-(trichloromethyl)pyridinium fluoroborate, and 40 ml of solvent was employed. There was a slight exotherm on mixing. The mixture was heated to 45° C. and allowed to react at that temperature for 3 hours. The mixture was then allowed to cool and the volatiles were removed by evaporation under reduced pressure. Analysis of the residue by standardized gas-liquid chromatography using a mass spectrometer detector indicated that the title product was present in 69 percent yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05164502 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-0adee789a9a74d829d2c29e23ffe00ca |
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| Source note | uspto-grants-1992_11 |
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