Hydrogen Bromide → (2R)-2-bromo-4-methylpentanoic acid

HRID 45912

Reaktionsgleichung

Reaktionsgleichung von HRID 45912
N[C@@H:2]([C:7]([OH:9])=[O:8])[CH2:3][CH:4]([CH3:6])[CH3:5].O.N([O-])=O.[Na+].[BrH:15]>>[Br:15][C@H:2]([CH2:3][CH:4]([CH3:6])[CH3:5])[C:7]([OH:9])=[O:8]

Komponenten

5

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

D-Leucine (8.2 g, 62.7 mmol) was dissolved in 3.0M HBr in water (99 mL, 0.3 mol) and cooled to 0° C. A solution of NaNO2 (6.9 g, 100 mmol) in water (11.3 mL, 627 mmol) was slowly added over 20 minutes. The mixture was stirred at 0° C. for 3 hours and then extracted twice with ethyl ether, washed with water then saturated aqueous NaCl, dried over MgSO4, filtered, and concentrated to afford (R)-2-bromo-4-methylpentanoic acid (11.5 g) as an off-yellow oil. This was taken on to the next step without further purification.

Aufarbeitung

  1. extractionextracted twice with ethyl ether
  2. washwashed with water
  3. dry with materialsaturated aqueous NaCl, dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-22037d73702f4e76aa4d49714ff01bb4
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08541597B2

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