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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Reactant | 4-Methylbenzene-1-sulfonic acid--(3R)-oxolan-3-amine (1/1) | HCID 14243169 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | (2S)-2-(4-bromophenyl)-4-[(1R)-1-phenylethyl]morpholine | HCID 50992522 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4-((1R)-1-phenylethyl)-(2S)-2-(4-(N-((3R)-tetrahydrofuran-3-yl)amino)phenyl)morpholine | HCID 66594454 | 53.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106045B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-78712ee937bd4d94b82eec3d1cabcf62 |
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| Source note | uspto-grants-2012_01 |
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