Pentane → (R)-Boc-N-Me-3-Amino-2-methylpropanoic acid

HRID 484352Notes

Reaction equation

HRID 484352 reaction equation
[C:1]([NH:8][CH2:9][CH:10]([CH3:14])[C:11]([OH:13])=[O:12])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[CH3:15]CCCC>C1COCC1>[CH3:15][N:8]([C:1]([O:3][C:4]([CH3:6])([CH3:7])[CH3:5])=[O:2])[CH2:9][C@@H:10]([CH3:14])[C:11]([OH:13])=[O:12]

Participants

4

Procedure

To a solution of N-Boc-α-(R,S)-methyl-β-alanine (1.33 g, 6.5 mmol) in THF (80 ml) was added pentane washed sodium hydride (1.2 g, 60% in oil dispersion) followed by methyl iodide (2 ml, exess). The reaction mixture was stirred overnight and then poured into an iced solution of citric acid (0.5N). The aqueous THF solution was extracted into ethyl acetate. Then the required acid was back extracted between ethyl acetate, sodium hydrogen carbonate and potassium hydrogen sulphate solutions. The organic extracts were dried (MgSO4) and evaporated to afford the title compound. (1.00 g, 71%), Anal: C10H19NO4.0.3H2O, Calc: C, 53.94; H, 8.87; N, 6.29. Found, C, 54.02; H, 8.56; N, 6.63.

Workup

  1. washwashed sodium hydride (1.2 g, 60% in oil dispersion)
  2. additionpoured into an iced solution of citric acid (0.5N)
  3. extractionThe aqueous THF solution was extracted into ethyl acetate
  4. extractionThen the required acid was back extracted between ethyl acetate, sodium hydrogen carbonate and potassium hydrogen sulphate solutions
  5. dry with materialThe organic extracts were dried (MgSO4)
  6. customevaporated

Sources & evidence

ORD record
ord-deb8fc75b1774abca656a63f44bacdd1
Source dataset
uspto-grants-1993_07
Patent number
US05231111

Reaction notes

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