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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246727Generated: November 2, 2026

Tetrabutylammonium Fluoride → HCID 68528780, compound

https://huagongshe.com/reaction/2246727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 68525183HCID 68525183—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68528780HCID 6852878084%

Reaction Steps

1′-[3-{[tert-butyl(dimethyl)silyl]oxy}-1-(3-fluorophenyl)propyl]spiro-[cyclohexane-1,3′-indol]-2′(1′H)-one (0.85 g, 1.82 mmol) was dissolved in tetrahydrofuran and tetrabutyl ammonium fluoride (1.0 M in THF, 3.64 mL, 3.64 mmol) was added and the mixture was stirred for 1 hour. Reaction was quenched with saturated aqueous ammonium chloride then saturated sodium bicarbonate was added, diluted with ether, washed with water, and saturated brine. The organic layer was separated, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude product was purified via Isco chromatography (Redisep, silica, gradient 0-100% ethyl acetate in hexane) to afford 0.54 g (84%) racemic 1′-[1-(3-fluorophenyl)-3-hydroxypropyl]spiro[cyclohexane-1,3′-indol]-2′(1′H)-one that was resolved by chiral HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687529B2
Source datasetuspto-grants-2010_03
ORD IDord-287dd8cc0cb34031a33498f554b5e829
Source noteuspto-grants-2010_03