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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | Ethyl 3-methyl-4-((triethylsilyl)ethynyl)benzoate | HCID 66874679 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-ethynyl-3-methylbenzoate | HCID 86652354 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09408907B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-bb9bb81da40c4059974096ecf5cbfa55 |
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| Source note | uspto-grants-2016_08 |
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