Reaktionsgleichung
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].O[C:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[C:16]([CH:23]=[O:24])=[CH:15][CH:14]=1.[CH3:25][O-:26].[Na+].[CH3:28]N(C=O)C>>[CH2:25]([O:26][C:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[C:16]([CH:23]=[O:24])=[CH:15][CH:14]=1)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH3:28]Komponenten
Reaktionsbedingungen
- Temperatur
- 50 °C
Versuchsvorschrift
To a solution of 1-bromodecane (10.0 g, 40.12 mmol) and 4-hydroxy-1-naphthaldehyde (6.29 g, 36.5 mmol) in anhydrous DMF (150 mL) was added NaOMe (2.38 g, 44.1 mmol). The mixture was stirred at 50° C. for 5 h. The reaction mixture was cooled to rt and concentrated under vacuo. The residue was dissolved in EtOAc and washed with brine (3×), dried over MgSO4, filtered and concentrated under reduced pressure to give an orange solid. Purification by chromatography (SiO2, c-Hex/EtOAc 9/1) gave the title product as a beige powder (11.12 g, 81%). 1H NMR (CDCl3, 300 MHz) δ 10.2 (s, 1H), 9.29 (d, 1H, J=8.7 Hz), 8.35 (d, 1H, J=8.7 Hz), 7.90 (d, 1H, J=8.3 Hz), 7.69 (m, 1H), 7.57 (m, 1H), 6.90 (d, 1H, J=7.9 Hz), 4.23 (t, 2H, J=6.4 Hz), 2.01-1.79 (m, 2H), 1.68-1.48 (m, 2H), 1.45-1.20 (m, 16H), 0.87 (m, 3H). HPLC (Condition A), Rt: 6.61 min (HPLC purity: 85.8%).
Aufarbeitung
- temperatureThe reaction mixture was cooled to rt
- concentrationconcentrated under vacuo
- dissolutionThe residue was dissolved in EtOAc
- washwashed with brine (3×)
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customto give an orange solid
- customPurification by chromatography (SiO2, c-Hex/EtOAc 9/1)
Quellen und Nachweise
- ORD-Eintrag
- ord-9c6226bdd3d14dd499bcbd305f0b9081
- Quelldatensatz
- uspto-grants-2009_09
- Patentnummer
- US07592477B2
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