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2-Amino-2-methyl-propionic acid ethyl ester hydrochloride

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2-Amino-2-methyl-propionic acid ethyl ester hydrochloride manufacturers

  • L-Aib-Oet.Hcl
  • L-Aib-Oet.Hcl pictures
  • 2026-09-30
  • CAS:17288-15-2
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T+
2-Amino-2-methyl-propionic acid ethyl ester hydrochloride Basic information
Product Name:2-Amino-2-methyl-propionic acid ethyl ester hydrochloride
Synonyms:H-AIB-OET HCL;H-AIB-OET HYDROCHLORIDE;H-ALPHA-ME-ALA-OET HCL;IFLAB-BB F2108-0015;2-AMINOISOBUTYRIC ACID ETHYL ESTER HYDROCHLORIDE;ALPHA-AMINOISOBUTYRIC ACID ETHYL ESTER HYDROCHLORIDE;2-Aminoisobutyric acid ethyl ester hydrochloride, 2-Methylalanine ethyl ester hydrochloride, alpha-Amino-2-methylbutyric acid ethyl ester hydrochloride, 2,2-Dimethylglycine ethylester hydrochloride;2-Amino-2-methyl-propionic acid ethyl ester hydrochloride
CAS:17288-15-2
MF:C6H14ClNO2
MW:167.63
EINECS:605-648-3
Product Categories:Pharmaceutical intermediate;Amino Acids & Derivatives;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:17288-15-2.mol
2-Amino-2-methyl-propionic acid ethyl ester hydrochloride Structure
2-Amino-2-methyl-propionic acid ethyl ester hydrochloride Chemical Properties
Melting point 156-157 °C
storage temp. Inert atmosphere,2-8°C
AppearanceWhite to off-white Solid
InChIInChI=1S/C6H13NO2.ClH/c1-4-9-5(8)6(2,3)7;/h4,7H2,1-3H3;1H
InChIKeyYREPHXXOTHNLEV-UHFFFAOYSA-N
SMILESC(OCC)(=O)C(C)(C)N.Cl
CAS DataBase Reference17288-15-2(CAS DataBase Reference)
Safety Information
MSDS Information
2-Amino-2-methyl-propionic acid ethyl ester hydrochloride Usage And Synthesis
UsesAs an amino acid derivative, 2-Amino-2-methyl-propionic acid ethyl ester hydrochloride can be used in pharmaceutical compositions.
UsesAn amino acid derivative used in pharmaceutical compositions.
Synthesis
2-Aminoisobutyric Acid

62-57-7

2-Amino-2-methyl-propionic acid ethyl ester hydrochloride

17288-15-2

Thionyl chloride (2.0 molar equivalents) was slowly added dropwise to a stirred solution of anhydrous ethanol (10.0 molar equivalents) pre-cooled to 0 °C under argon protection. The reaction temperature was maintained at 0 °C with continuous stirring for 1 hour and then gradually warmed up to room temperature. Subsequently, 2-aminoisobutyric acid (1.0 molar equivalent) was added and the reaction mixture was heated to reflux overnight. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and finally the residual trace solvent was removed by azeotropic distillation. The crude product was ground with ether to give purified ethyl 2-aminoisobutyrate hydrochloride. In Example 14, ethyl 2-aminoisobutyrate hydrochloride (Product 14n) was prepared according to the method of Example 1 (A) as a white solid (9.12 g, 776.0 mmol) from 2-aminoisobutyric acid (8.0 g, 77.6 mmol), thionyl chloride (11.3 mL, 155.2 mmol) and anhydrous ethanol (45.5 mL, 776.0 mmol). (70% yield). Its 1H-NMR (CDCl3; 300 MHz) and 13C-NMR (CDCl3; 75 MHz) data were consistent with the expected structure.

References[1] Patent: US2007/42988, 2007, A1. Location in patent: Page/Page column 18; 22
[2] Patent: US6028032, 2000, A
2-Amino-2-methyl-propionic acid ethyl ester hydrochloride Preparation Products And Raw materials
Raw materials2-Aminoisobutyric Acid
Preparation ProductsEthyl 2-hydroxyisobutyrate-->Methacrylic acid-->Alanine, 2-methyl-N-(phenylmethyl)-, ethyl ester-->2-Methyl-N-(phenylmethylene)alanine Ethyl Ester
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