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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823124Generated: October 31, 2026

Tetrabutylammonium Fluoride → HCID 24824075, compound

https://huagongshe.com/reaction/1823124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 24823941HCID 24823941—
SolventTetrahydrofuranHCID 8028—
ProductHCID 24824075HCID 2482407573.4%

Reaction Steps

To a solution of [4-[2-[N-benzyl-N-[(2R)-2-[[tert-butyl (dimethyl) silyl]oxy]-2-(3-chlorophenyl) ethyl]amino]-ethyl]phenyl][4-[[tert-butyl(dimethyl)silyl]oxy]phenyl]-methanol (1.1 g) in tetrahydrofuran (15 ml) was added 1M tetrabutylammonium fluoride in tetrahydrofuran (5.0 ml) at 0° C., and the mixture was stirred at room temperature for 24 hours under nitrogen. The mixture was partitioned between ethyl acetate and water. The organic layer was separated, washed with water and brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=2/1) to give 4-[[4-[2-[N-benzyl-N-[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]ethyl]-phenyl](hydroxy)methyl]phenol (550 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037938B2
Source datasetuspto-grants-2006_05
ORD IDord-f7fc24cc007941a7a63e83164745c21a
Source noteuspto-grants-2006_05