Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Reactant | 2-(2,3,4,5,6-Pentafluorophenyl)oxirane | HCID 2775981 | — |
| Product | HCID 15113981 | HCID 15113981 | 31.9% |
Reaction Steps
To Teflon vessel containing 4.2 g (22.5 mmol)of tributylamine was cooled in a dry-ice methanol bath, and to this was added dropwise 2.3 g (112.5 mmol) of anhydrous hydrogen fluoride to prepare 6.4 g (22.5 mmol) of n-Bu3N.5HF. To this was added dropwise 3.15 g (15 mmol) of (+)-pentafluorostyrene oxide at 0° C., and was stirred for 10 hours at 40° C. After it was left to cool, the same treatment as that provided in Example 16 gave 1.1 g of (+)-2-fluoro-2-(pentafluorophenyl)ethanol. Its GC purity was 96%, while its [α]D25 was +10.8° (c=0.54, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05041641 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-6ccf8177470244969e36bb77eacc33b8 |
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| Source note | uspto-grants-1991_08 |
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