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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424430Generated: October 30, 2026

2-(Di-tert-butylphosphino)biphenyl → 4-((1R)-1-phenylethyl)-(2S)-2-(4-(N-((3R)-tetrahydrofuran-3-yl)amino)phenyl)morpholine

https://huagongshe.com/reaction/424430

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Reactant4-Methylbenzene-1-sulfonic acid--(3R)-oxolan-3-amine (1/1)HCID 14243169—
ReactantSodium t-butoxideHCID 23676156—
Reactant(2S)-2-(4-bromophenyl)-4-[(1R)-1-phenylethyl]morpholineHCID 50992522—
Catalystpalladium(II) acetateHCID 167845—
Solventtert-ButanolHCID 6386—
Product4-((1R)-1-phenylethyl)-(2S)-2-(4-(N-((3R)-tetrahydrofuran-3-yl)amino)phenyl)morpholineHCID 6659445453.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

(R)-(+)-3-Aminotetrahydrofuran toluene-4-sulfonate (2.0 g, 7.7 mmol) was added to a suspension of (2S)-2-(4-bromophenyl)-4-((1R)-1-phenylethyl)morpholine (2.4 g, 6.9 mmol), palladium acetate (65 mg, 0.29 mmol), 2-(di-t-butylphosphino)biphenyl (170 mg, 0.57 mmol), and sodium tert-butoxide (3.4 g, 35.4 mmol) in tert-butanol (50 ml) at room temperature. After heating at 90° C. for 6 hours, the resulting suspension was passed through a Celite column. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel chromatography eluting 5-10% methanol in chloroform to afford 4-((1R)-1-phenylethyl)-(2S)-2-(4-(N-((3R)-tetrahydrofuran-3-yl)amino)phenyl)morpholine (1.3 g, 53%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106045B2
Source datasetuspto-grants-2012_01
ORD IDord-78712ee937bd4d94b82eec3d1cabcf62
Source noteuspto-grants-2012_01