HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760631Generated: October 29, 2026
Tetrabutylammonium Fluoride → 4-Hydroxy-2-methylbenzofuran
https://huagongshe.com/reaction/1760631
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 4-t-Butyldimethylsilyloxy-2-methylbenzofuran | HCID 22595863 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Hydroxy-2-methylbenzofuran | HCID 12174561 | 96% |
Reaction Steps
A solution of the crude 4-t-butyldimethylsilyloxy-2-methylbenzofuran (1.822 g, 6.99 mmol) in THF (28 mL) and cooled to 0° C. (ice water bath) was treated with TBAF (14 mL, 13.00 mmol, 1.0 M in THF). After 30 min. the solution was concentrated under reduced pressure and diluted with 150 mL of Et2O and 300 mL of H2O in a separatory funnel. The mixture was shaken and separated in a separatory funnel. The aqueous layer was extracted with Et2O (2×125 mL). The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The residue was passed through a column of silica gel [5 to 20% EtOAc/hexanes] and concentrated under reduced pressure to give the product as a white solid (0.9923 g. 96%). A portion (0.052 g) of the material was purified by silica gel chromatography [5 to 20% EtOAc/hexanes] to give the product as a white solid (0.0382 g, 73% recovery). C9H8O2.0.3H2O
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06844344B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-3511274f576a47b195c7d565f8df395f |
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| Source note | uspto-grants-2005_01 |
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