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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920167Generated: October 31, 2026

Tetrabutylammonium Fluoride → HCID 68920313, compound

https://huagongshe.com/reaction/1920167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 68922812HCID 68922812—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 68920313HCID 68920313100%

Reaction Steps

To a solution of (3S,5R)-benzyl 3-(tert-butoxycarbonylamino)-5-(tert-butyldimethylsilyloxy)piperidine-1-carboxylate (1 eq) in 30 mL of THF was added 5.2 mL of TBAF (1.2 eq). The reaction mixture was stirred at room temperature for 2 hours. The mixture was diluted with ethyl acetate, washed with brine, then dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (5% methanol in EtOAc:hexanes=1:1) to yield (3S,5R)-benzyl 3-(tert-butoxycarbonylamino)-5-hydroxypiperidine-1-carboxylate (100%). LC/MS (m/z): 251.2 (MH+), Rt: 0.89. HPLC: Rt: 3.26 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168794B2
Source datasetuspto-grants-2012_05
ORD IDord-908cec65a85b49159e7e5188ec8aaffb
Source noteuspto-grants-2012_05