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H-ABU-OME HCL

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H-ABU-OME HCL Basic information

Product Name:
H-ABU-OME HCL
Synonyms:
  • (S)-2-Aminobutanoic Acid Methyl Ester HCl
  • (S)-2-AMinobutanoic Acid Methyl Ester Hydrochloride
  • (S)-2-AMino-butanoic Acid Methyl Ester Hydrochloride
  • L-α-AMinobutyric Acid Methyl Ester Hydrochloride
  • Methyl (2S)-2-aminobutanoate hydrochloride
  • Methyl (S)-2-aminobutanoate hydrochloride
  • Methyl (S)-2-aminobutyrate hydrochloride
  • Methyl L-2-aminobutanoate hydrochloride
CAS:
56545-22-3
MF:
C5H12ClNO2
MW:
153.60728
Product Categories:
  • Amino Acids & Derivatives
  • Chiral Reagents
Mol File:
56545-22-3.mol
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H-ABU-OME HCL Chemical Properties

Melting point:
116-117℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
Aqueous Acid (Sparingly), DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
White to Off-White
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H-ABU-OME HCL Usage And Synthesis

Uses

Intermediate in the preparation of Ergonovine (E597800) derivatives.

Synthesis

67-56-1

34306-42-8

7682-18-0

The general procedure for the synthesis of DL-2-aminobutyric acid methyl ester hydrochloride from methanol and Boc-L-2-aminobutyric acid was as follows: 10.0 g (49.2 mmol) of Boc-L-2-aminobutyric acid was dissolved in 100 mL of methanol, and 6 mL (82.2 mmol) of thionyl chloride was added slowly and dropwise at 0 °C. The reaction mixture was stirred at room temperature for 14 h before the solvent was removed by vacuum evaporation. A product of 7.6 g (101% yield) was obtained. The structure of the product was confirmed by electrospray mass spectrometry (ES-MS) and the molecular ion peak (M + H)+ was observed as 118.

References

[1] Patent: US2010/144681, 2010, A1. Location in patent: Page/Page column 67

H-ABU-OME HCLSupplier

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