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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348565Generated: October 31, 2026

Trifluoroacetic acid → 4-Morpholinopiperidine

https://huagongshe.com/reaction/1348565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMorpholineHCID 8083—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium cyanoborohydrideHCID 5003444—
CatalystHCID 178460666HCID 178460666—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-MorpholinopiperidineHCID 795724—

Reaction Steps

To a stirred solution of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (Aldrich, 3.0 g, 15 mmol) in THF (25 mL), morpholine (Aldrich, 1.56 g, 18 mmol) and Ti(OiPr)4 (Aldrich, 5.58 mL) were added successively and the mixture was stirred at room temperature for 1 hour. Then, 15 mL of ethanol was added and followed by sodium cyanoborohydride (0.63 g, 10.05 mmol). The resulting mixture was stirred at room temperature over night and the reaction was quenched with addition of water (4 mL). The mixture was stirred for 30 minutes and the white solid was filtered out and the filtrate was evaporated. The residue was partitioned between ether and water and the organic layer was separated and dried with sodium sulfate. Removal of solvent gave a white solid which was treated with 40 mL of 50% TFA in methylene chloride. The solution was stirred at room temperature for 1 hour and the solvent was removed. The residue was lyophilized to give a white solid. 5.48 g, 98%. MS (m+H)+: 171.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211576B2
Source datasetuspto-grants-2007_05
ORD IDord-fb13433e86294b4590b2bf02664e294d
Source noteuspto-grants-2007_05