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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479617Generated: October 26, 2026

Tetrabutylammonium Fluoride → Methyl 4-ethynyl-3-methylbenzoate

https://huagongshe.com/reaction/1479617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantMethyl 3-methyl-4-((triethylsilyl)ethynyl)benzoateHCID 66875322—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-ethynyl-3-methylbenzoateHCID 85602522—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 3-methyl-4-((triethylsilyl)ethynyl)benzoate (from the previous step) (1.0 eq.) in THF (0.2 M), was added TBAF (0.2 eq.) slowly at 0° C. Then the reaction mixture was stirred at 0° C. for 1 hour. After warmed to ambient temperature, the reaction mixture was diluted with ethyl acetate and water. The two phases were separated, and the aqueous layer was extracted twice with ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vaccuo. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give methyl 4-ethynyl-3-methylbenzoate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-8189267c5356451a845997714dc730ff
Source noteuspto-grants-2016_08