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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2,2,2-Trifluoro-N-{2-fluoro-5-[(trimethylsilyl)ethynyl]phenyl}acetamideHCID 59511383—
SolventTetrahydrofuranHCID 8028—
ProductN-(5-ethynyl-2-fluorophenyl)-2,2,2-trifluoroacetamideHCID 59511405—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812022B2
Source datasetuspto-grants-2010_10
ORD IDord-bc466bcd1f6e4e45be74502f78d10c2f
Source noteuspto-grants-2010_10