HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908900Generated: October 28, 2026
TBAF tetrahydrofuran → HCID 57414919, compound
https://huagongshe.com/reaction/1908900
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | TBAF tetrahydrofuran | HCID 11078149 | — |
| Reactant | HCID 59342562 | HCID 59342562 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57414919 | HCID 57414919 | 88% |
Reaction Steps
To a solution of methyl {(3S)-6-[(4′-{[tert-butyl(dimethyl)silyl]oxy}-3′-chloro-2′,6′-dimethylbiphenyl-3-yl)methoxy]-2,3-dihydro-1-benzofuran-3-yl}acetate (2.01 g, 3.54 mmol) in tetrahydrofuran (20 mL) was added 1 M tetrabutylammonium fluoride tetrahydrofuran solution (3.9 mL, 3.9 mmol) at room temperature, and the mixture was stirred at the same temperature for 3 hr under nitrogen atmosphere. The reaction mixture was concentrated under reduced pressure, water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=10:90-50:50) to give the title compound (1.41 g, yield 88%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598226B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-604bd94438d94c40a156d8edad96c82c |
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| Source note | uspto-grants-2013_12 |
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