H-ABU-OME HCL
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
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
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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H-ABU-OME HCL(56545-22-3)Related Product Information
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- 2-AMINO-2-METHYL-BUTYRIC ACID METHYL ESTER HYDROCHLORIDE
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