HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876375Generated: October 29, 2026
Triethylamine → 2-Fluoro-1-(2-fluoro-phenyl)-ethanone
https://huagongshe.com/reaction/876375
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Perfluoro-1-butanesulfonyl fluoride | HCID 67814 | — |
| Reactant | N,N-Diethylethanamine trihydrofluoride | HCID 175505 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21837678 | HCID 21837678 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Fluoro-1-(2-fluoro-phenyl)-ethanone | HCID 21964491 | 61% |
Reaction Steps
A solution of 1-(2-fluorophenyl)-2-hydroxyethanone [CAS 218771-68-7; WO9857925, ex. 16) (2.77 g, 18.0 mmol) in dichloromethane (42 ml) was treated consecutively at 0° C. with triethylamine (6.36 g, 62.8 mmol), triethylamine trihydrofluoride (3.05 g, 18.0 mmol) and nonafluoro-n-butanesulfonyl fluoride (8.48 g, 26.9 mmol). The tube was sealed and the reaction mixture stirred overnight at room temperature. For the workup, the dark red solution was poured on a saturated solution of sodium hydrogencarbonate and ice, then extracted with dichloromethane. The organic layer was separated, dried over sodium sulphate and evaporated. The crude material was purified by flash chromatography on silica gel (Telos Flash Silica) using dichloromethane as the eluent to give the 2-fluoro-1-(2-fluoro-phenyl)-ethanone (1.23 g, 61% yield) as a yellow semisolid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987255B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-58ba0cfb4d7a49438f29a8ede9b4c0ff |
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| Source note | uspto-grants-2015_03 |
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