HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159985Generated: October 30, 2026
Tetrabutylammonium Fluoride → N-(5-ethynyl-2-fluorophenyl)-2,2,2-trifluoroacetamide
https://huagongshe.com/reaction/1159985
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 2,2,2-Trifluoro-N-{2-fluoro-5-[(trimethylsilyl)ethynyl]phenyl}acetamide | HCID 59511383 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(5-ethynyl-2-fluorophenyl)-2,2,2-trifluoroacetamide | HCID 59511405 | — |
Reaction Steps
A solution of 2,2,2-trifluoro-N-{2-fluoro-5-[(trimethylsilyl)ethynyl]phenyl}acetamide (5.3 g, 17 mmol) in THF (400 mL) was cooled to 0° C., and a 1.0 M solution of TBAF in THF (17 mL, 17 mmol) was added dropwise. The resulting mixture was stirred for 10 min. at 0° C. The reaction was quenched with H2O (150 mL), concentrated under reduced pressure, and extracted with DCM. The combined organic layers were concentrated under reduced pressure, and the crude solid was used in the next reaction without further purification. ES-LC/MS m/z=230 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812022B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-bc466bcd1f6e4e45be74502f78d10c2f |
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| Source note | uspto-grants-2010_10 |
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