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

HRID 338816

反応式

HRID 338816 の反応式
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]

参加物

5

反応条件

温度
0 °C

実験手順

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.

後処理

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

出典と根拠

ORDレコード
ord-6325552a65ea474897b31ac4ccefe38c
出典データセット
uspto-grants-2014_11
特許番号
US08889882B2

関連ノート

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