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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697249Generated: October 29, 2026

Tetrabutylammonium Fluoride → HCID 59347043, compound

https://huagongshe.com/reaction/1697249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(4S,5S)-Tert-butyl 5-((tert-butyldimethylsilyloxy)methyl)-4-((2-chloro-6-methylpyridin-4-yl)methyl)-2,2-dimethyloxazolidine-3-carboxylateHCID 86614126—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59347043HCID 59347043—

Reaction Conditions

Temperature0 °C

Reaction Steps

(4S,5S)-Tert-butyl 5-((tert-butyldimethylsilyloxy)methyl)-4-((2-chloro-6-methylpyridin-4-yl)methyl)-2,2-dimethyloxazolidine-3-carboxylate (0.206 g, 0.425 mmol) was dissolved in THF (4 mL) and cooled to 0° C. TBAF (0.637 ml, 0.637 mmol) was added to the mixture dropwise and the reaction was stirred 1 hr and then quenched with saturated ammonium chloride and diluted with EtOAc. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with water, brine, dried over sodium sulfate, and concentrated. The crude material was purified by silica column chromatography (19:1 DCM/MeOH) and then reverse phase HPLC to give the title compound. MS m/z: 371.3 (100%, M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163909B2
Source datasetuspto-grants-2012_04
ORD IDord-9dd4917a1eef4a96aab65ca2ef5b611a
Source noteuspto-grants-2012_04