1-Bromo-2-methylpropane → HCID 59214340, Verbindung

HRID 2192483Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2192483
[OH:1][C:2]1[CH:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:5]=[CH:4][N:3]=1.[H-].[Na+].Br[CH2:15][CH:16]([CH3:18])[CH3:17]>CN(C)C=O>[CH3:15][CH:16]([CH3:18])[CH2:17][N:3]1[CH:4]=[CH:5][C:6]([C:8]([O:10][CH3:11])=[O:9])=[CH:7][C:2]1=[O:1]

Komponenten

5

Versuchsvorschrift

To a solution of methyl 2-hydroxy-4-pyridinecarboxylate (D26; 1.02 g, 6.66 mmol) in N,N-dimethylformamide (20 ml) was added sodium hydride (60%; 0.293 g, 7.33 mmol). The resulting solution was stirred at room temperature for 15 mins. 1-Bromo-2-methylpropane (0.87 ml, 7.99 mmol) was then added and the mixture was stirred at 80° C. for 2 hrs. The reaction was quenched with methanol and the solvent was removed under vacuum. The residue was partitioned between ethyl acetate and water, the organic layer dried over magnesium sulphate and concentrated under vacuum. The crude material was purified by chromatography on silica, eluting with 50-80% ethyl acetate in cyclohexane gave the title compound as a light blue solid (450 mg). MS: m/z 210 [MH+]. O-alkylated material was also isolated.

Aufarbeitung

  1. stirringthe mixture was stirred at 80° C. for 2 hrs
  2. customThe reaction was quenched with methanol
  3. customthe solvent was removed under vacuum
  4. customThe residue was partitioned between ethyl acetate and water
  5. dry with materialthe organic layer dried over magnesium sulphate
  6. concentrationconcentrated under vacuum
  7. customThe crude material was purified by chromatography on silica
  8. washeluting with 50-80% ethyl acetate in cyclohexane

Quellen und Nachweise

ORD-Eintrag
ord-c9653ae70ade4397b6d719e971955dff
Quelldatensatz
uspto-grants-2012_12
Patentnummer
US08329730B2

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