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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424416Generated: October 30, 2026

Benzophenone imine → HCID 66594463, compound

https://huagongshe.com/reaction/424416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenone imineHCID 136809—
ReactantSodium t-butoxideHCID 23676156—
Reactant(2S)-2-(4-bromophenyl)-4-[(1R)-1-phenylethyl]morpholineHCID 50992522—
Catalyst2-(Di-tert-butylphosphino)biphenylHCID 2734215—
CatalystPalladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1)HCID 11029508—
SolventTolueneHCID 1140—
ProductHCID 66594463HCID 6659446396%

Reaction Steps

A solution of (2S)-2-(4-bromophenyl)-4-((1R)-l-phenylethyl)morpholine (15.6 g, 45 mmol), benzophenone imine (9 g, 50 mmol), tris(dibenzylideneacetone)-dipalladium(0)-chloroform adduct (0.93 g, 0.9 mmol), sodium tert-butoxide (6.0 g, 63 mmol) and 2-(di-t-butylphosphino)biphenyl (0.53 g, 1.8 mmol) in toluene (135 ml) was stirred at 95° C. for 4 hours. The solvent was removed in vacuo and the residue was partitioned between water and ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. To a solution of the resulting residue in tetrahydrofuran (180 ml) was added 6N hydrochloric acid (180 ml) and the mixture was stirred at room temperature for one hour. The solvent was removed in vacuo and the residue was partitioned between water and ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated. The resulting residue was purified by column chromatography on silica gel (hexane-AcOEt, 2:1) to give (2S)-2-(4-aminophenyl)-4-((1R)-1-phenylethyl)morpholine (12.2 g, 96%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106045B2
Source datasetuspto-grants-2012_01
ORD IDord-c15ce97ac0f44afea4cbac1521cd1c6c
Source noteuspto-grants-2012_01