Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-Bromo-5-fluorobenzaldehyde | HCID 2773321 | — |
| Reactant | HCID 24781137 | HCID 24781137 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58572501 | HCID 58572501 | 79% |
Reaction Steps
With reference to Chirality, 2005, 17, 476-480, 1.06 M solution of diethyl zinc in hexane (18.6 ml, 19.7 mmol) was added dropwise under ice cooling to a solution of 1-[(S)-(2-methoxy phenyl){[(1S)-1-phenylethyl]amino}methyl]-2-naphthol (0.38 g, 0.99 mmol) in toluene (5 ml). The mixture was stirred at room temperature for 1 hour. After stirring, the mixture was added with 2-bromo-5-fluorobenzaldehyde (2.0 g, 9.85 mmol) under ice cooling and stirred at room temperature for 16 hours. The reaction solution was added with 1 N aqueous hydrochloride solution and extracted with dichloromethane. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (hexane/ethyl acetate=5/1) to give the title compound as a transparent oily substance (1.81 g, yield 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183272B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-1b5e730a78ce4f018acbf4e14fc9b786 |
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| Source note | uspto-grants-2012_05 |
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