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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453446Generated: October 30, 2026

TBAF tetrahydrofuran → HCID 57414919, compound

https://huagongshe.com/reaction/453446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTBAF tetrahydrofuranHCID 11078149—
ReactantHCID 59342562HCID 59342562—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57414919HCID 5741491988%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492430B2
Source datasetuspto-grants-2013_07
ORD IDord-8c87096fa3c64f40abe94274de0a8398
Source noteuspto-grants-2013_07