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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555797Generated: October 30, 2026

Tetrabutylammonium Fluoride → HCID 59351436, compound

https://huagongshe.com/reaction/555797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 66986197HCID 66986197—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59351436HCID 59351436—

Reaction Steps

To a stirred solution of 1-benzyl-4-(1,1,1-trifluoro-2-(trimethylsilyloxy)propan-2-yl)piperidine (3 g, 8.3 mmol) in THF (30 mL), tetrabutylammonium fluoride (3.2 g, 12.4 mmol) was added slowly at RT. The reaction mixture was stirred for 3 h. After completion of the reaction, the mixture was quenched with saturated ammonium chloride solution, extracted with ethyl acetate. The organic layer was washed with brine solution and dried over anhydrous sodium sulfate and concentrated under vacuum to afford 2-(1-benzylpiperidin-4-yl)-1,1,1-trifluoropropan-2-ol product. [M+1]=288.15

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053438B2
Source datasetuspto-grants-2011_11
ORD IDord-79abcc9acdad4228869a3887e4361d52
Source noteuspto-grants-2011_11