Methyl chloroformate → 2-((Methoxycarbonyl)amino)-3-methylbutanoic acid

HRID 79970Notes

Reaction equation

HRID 79970 reaction equation
[NH2:1][C@@H:2]([C:6]([OH:8])=[O:7])[CH:3]([CH3:5])[CH3:4].C(=O)([O-])[O-].[Na+].[Na+].Cl[C:16]([O:18][CH3:19])=[O:17]>[OH-].[Na+].O>[CH3:19][O:18][C:16]([NH:1][CH:2]([CH:3]([CH3:5])[CH3:4])[C:6]([OH:8])=[O:7])=[O:17]

Participants

6

Conditions

Temperature
0 °C

Procedure

To a solution of d-valine, (5.0 g) in 1N sodium hydroxide (42.7 mL) was added sodium carbonate (4.53 g). The solution was cooled to 0° C. and methyl chloroformate (0.289 mL) was added dropwise over 2 h and reaction mixture was stirred for 2 h at 0° C. White reaction mixture was diluted with enough H2O to form a colorless solution and washed with ethyl ether (3×30 mL). Aqueous layer was acidified to pH=2 with concentrated HCl to give a white precipitate that collected by filtration, washed with H2O and dried under high vacuum to give 2-Methoxycarbonylamino-3-methyl-butyric acid as a crystalline white solid (4.668 g). LCMS-ESI−: calc'd for C7H13NO4: 176.2 (M+H+). Found: 175.9 (M+H+).

Workup

  1. customreaction mixture
  2. customWhite reaction mixture
  3. customto form a colorless solution
  4. washwashed with ethyl ether (3×30 mL)
  5. customto give a white precipitate
  6. filtrationthat collected by filtration
  7. washwashed with H2O
  8. customdried under high vacuum

Sources & evidence

ORD record
ord-21fafb7ca61c4c13952b86c4e0a9159d
Source dataset
uspto-grants-2014_09
Patent number
US08841278B2

Reaction notes

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