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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478398Generated: October 30, 2026

Morpholine → Rac-cis-4-(1-benzyl-3-phenyl-piperidin-4-yl)-morpholine

https://huagongshe.com/reaction/478398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-Benzyl-3-phenylpiperidin-4-oneHCID 11817956—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductRac-cis-4-(1-benzyl-3-phenyl-piperidin-4-yl)-morpholineHCID 13172414854.2%

Reaction Steps

To a mixture of 1-benzyl-3-phenyl-piperidin-4-one (2.07 g, 7.78 mmol) and morpholine (678 mg, 7.78 mmol) was added tetraisopropyl-orthotitanate (2.97 mL, 9.73 mmol) at room temperature. After stirring at room temperature overnight the reaction mixture was diluted with ethanol (8.0 mL) and sodium cyanoborohydride (369 mg, 5.37 mmol) was added. The reaction mixture was stirred at room temperature for 24 h and was diluted with water (2.0 mL). The inorganic precipitate was filtered off and washed with ethanol. The filtrate was evaporated and purified by flash chromatography on silica gel with toluene/ethyl acetate 6:1 to give rac-cis-4-(1-benzyl-3-phenyl-piperidin-4-yl)-morpholine (1.42 g, 54%) as a yellow solid, MS: m/e=337.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642226B2
Source datasetuspto-grants-2003_11
ORD IDord-2e969a9dfac24666a95fabd8ef61fc44
Source noteuspto-grants-2003_11