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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043793Generated: October 31, 2026

Trifluoroacetic acid → 4-(2-Methoxy-4-nitrophenoxy)piperidine

https://huagongshe.com/reaction/1043793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 18542820HCID 18542820—
SolventDichloromethaneHCID 6344—
Product4-(2-Methoxy-4-nitrophenoxy)piperidineHCID 5503615496%

Reaction Steps

Trifluoroacetic acid (5 eq) was added to a solution of tert-butyl 4-(2-methoxy-4-nitrophenoxy)piperidine-1-carboxylate (200 mg, 0.57 mmol, 1 eq) in dichloromethane, stirring at room temperature for 1 hour. The solvent was then evaporated, the residue was brought to pH 10 with sat. aq. Na2CO3 solution and extracted with EtOAc. The organic layer was washed with brine, dried over sodium sulfate and evaporated to afford the product 4-(2-methoxy-4-nitrophenoxy)piperidine as a light yellow solid (137.3 mg, 96%). LC/MS (m/z): 253.2 (MH+), Rt 1.81 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563549B2
Source datasetuspto-grants-2013_10
ORD IDord-e6f1649cf6e742d29c3ecc1956588c0d
Source noteuspto-grants-2013_10