Acetaldehyde → HCID 9947152, Verbindung

HRID 1795582Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1795582
[CH3:1][C:2]1[C:3]([NH:15][C:16]2[CH:24]=[CH:23][C:19]([C:20]([O-:22])=[O:21])=[CH:18][CH:17]=2)=[CH:4][C:5]2[C:6]([CH3:14])=[CH:7][CH2:8][C:9]([CH3:13])([CH3:12])[C:10]=2[CH:11]=1.[CH2:25]1COC[CH2:26]1.[CH:30](=O)C.[BH3-]C#N.[Na+]>C(OCC)(=O)C.O.C(O)(=O)C>[CH2:14]([C:6]1[C:5]2[CH:4]=[C:3]([NH:15][C:16]3[CH:17]=[CH:18][C:19]([C:20]([O:22][CH2:25][CH3:26])=[O:21])=[CH:23][CH:24]=3)[C:2]([CH3:1])=[CH:11][C:10]=2[C:9]([CH3:12])([CH3:13])[CH2:8][CH:7]=1)[CH3:30]

Komponenten

8

Versuchsvorschrift

General Procedure D To a solution of 4-[(3,5,5,8-Tetramethyl-5,6-dihydronaphthalen-2-yl)amino]benzoate (Compound 15, 0.20 g, 0.58 mmol) and 5 mL of THF was added acetaldehyde (0.30 mL, 5.8 mmol), followed by NaBH3CN (0.10 g, 1.74 mmol) and glacial acetic acid (2 mL). The resulting reaction mixture was stirred at room temperature for 24 h, then treated with water and ethyl acetate. The layers were separated, and the aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with NaHCO3 1 N, brine, and dried over MgSO4, and filtered. The solvent was removed, and the residue was purified by flash column (hexane:ethyl acetate=4:1) to give 0.19 g (88%) of the title compound as a light yellow solid.

Aufarbeitung

  1. customThe resulting reaction mixture
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted three times with ethyl acetate
  4. washThe combined organic layers were washed with NaHCO3 1 N, brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customThe solvent was removed
  8. customthe residue was purified by flash column (hexane:ethyl acetate=4:1)

Quellen und Nachweise

ORD-Eintrag
ord-6b1e579f68e94edb9f6923d309b065c4
Quelldatensatz
uspto-grants-2006_04
Patentnummer
US07026487B2

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