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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855148Generated: October 31, 2026

Trifluoroacetic acid → Ethyl (2S,5R)-5-((benzyloxy)amino)piperidine-2-carboxylate

https://huagongshe.com/reaction/1855148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(2S,5R)-1-tert-butyl 2-ethyl 5-((benzyloxy)amino)piperidine-1,2-dicarboxylateHCID 86700665—
SolventDichloromethaneHCID 6344—
ProductEthyl (2S,5R)-5-((benzyloxy)amino)piperidine-2-carboxylateHCID 8667500595%

Reaction Steps

TFA (600 mL) was added to a solution of (2S,5R)-1-tert-butyl 2-ethyl 5-((benzyloxy)amino)piperidine-1,2-dicarboxylate (263 g, 0.7 mol) in DCM (600 mL) at 20° C. The mixture was stirred at rt overnight and then concentrated in vacuum. The crude product was adjusted to pH 10 with sat. NaHCO3 solution, and then extracted with DCM three times. The combined organic layer was concentrated in vacuum and purified by silica gel column chromatography (20:1 DCM/MeOH) to afford (2S,5R)-ethyl 5-((benzyloxy)amino)piperidine-2-carboxylate (184.9 g, 95%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962843B2
Source datasetuspto-grants-2015_02
ORD IDord-e63a3210363c40f3a229502a9fe4a15a
Source noteuspto-grants-2015_02