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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479573Generated: October 31, 2026

Tetrabutylammonium Fluoride → Ethyl 4-ethynyl-3-methylbenzoate

https://huagongshe.com/reaction/1479573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantEthyl 3-methyl-4-((triethylsilyl)ethynyl)benzoateHCID 66874679—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-ethynyl-3-methylbenzoateHCID 86652354—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl 3-methyl-4-((triethylsilyl)ethynyl)benzoate (from the previous step) (1.0 eq.) in THF (0.3 M) at 0° C. was added dropwise 1.0 M TBAF in THF (1.2 eq.). After stirring for 10 minutes at 0° C., the reaction was quenched with saturated aqueous sodium bicarbonate solution. The two phases were separated, and the aqueous layer was extracted with ether. 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 0-5% ethyl acetate in hexane to give ethyl 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-bb9bb81da40c4059974096ecf5cbfa55
Source noteuspto-grants-2016_08