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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | Methyl 3-methyl-4-((triethylsilyl)ethynyl)benzoate | HCID 66875322 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-ethynyl-3-methylbenzoate | HCID 85602522 | — |
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
| 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-8189267c5356451a845997714dc730ff |
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| Source note | uspto-grants-2016_08 |
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