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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779012Generated: October 30, 2026

Tetrabutylammonium Fluoride → Methyl 2-(2-ethynyl-4-fluorophenyl)acetate

https://huagongshe.com/reaction/1779012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantMethyl 2-(4-fluoro-2-((trimethylsilyl)ethynyl)phenyl)acetateHCID 59457720—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(2-ethynyl-4-fluorophenyl)acetateHCID 86712664—

Reaction Steps

A solution of TBAF (1.0 M in THF; 2.0 mL, 2.0 mmol) was added to a stirred solution of methyl 2-(4-fluoro-2-((trimethylsilyl)ethynyl)phenyl)acetate (A49) (0.212 g, 0.802 mmol) in DCM (5 mL). After 2 minutes the resulting mixture was diluted with water (100 mL) and DCM (50 mL). The organic fraction was separated and adsorbed onto silica gel then purified using column chromatography (Biotage Isolera, 12 g SiO2 Cartridge, 0-20% EtOAc in petroleum benzine 40-60° C.) to give the title compound A50 as a brown oil (0.106 g, 69%); 1H NMR (400 MHz, CDCl3) δ 7.37-7.26 (m, 1H), 7.23 (dd, J=9.0, 2.8 Hz, 1H), 7.06 (m, 1H), 3.84 (s, 2H), 3.73 (s, 3H), 3.33 (s, 1H). LCMS-A: rt 5.838 min; m/z 193 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266864B2
Source datasetuspto-grants-2016_02
ORD IDord-c963d9eb1db748eea4a94d293955aacb
Source noteuspto-grants-2016_02