Ethyl L-valinate hydrochloride
Ethyl L-valinate hydrochloride Basic information
- Product Name:
- Ethyl L-valinate hydrochloride
- Synonyms:
-
- H-VAL-OET HCL
- H-VAL-OET HYDROCHLORIDE
- (L)-ETHYL 2-AMINO-3-METHYLBUTANOATE HYDROCHLORIDE
- ETHYL 2-AMINO-3-METHYLBUTANOATE HYDROCHLORIDE
- L-VALINE ETHYL ESTER HCL
- L-VALINE ETHYL ESTER HYDROCHLORIDE
- VALINE-OET HCL
- H-VAL-OET·HCL
- CAS:
- 17609-47-1
- MF:
- C7H16ClNO2
- MW:
- 181.66
- EINECS:
- 241-580-7
- Product Categories:
-
- Valine [Val, V]
- Amino hydrochloride
- Amino Acid Derivatives
- Peptide Synthesis
- Valine
- Amino Acids
- Amino Acid Derivatives
- Mol File:
- 17609-47-1.mol
Ethyl L-valinate hydrochloride Chemical Properties
- Melting point:
- 102-105 °C(lit.)
- alpha
- 7 º (c=2, H2O)
- storage temp.
- Sealed in dry,Room Temperature
- Water Solubility
- Soluble in water
- solubility
- Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
- form
- powder to crystal
- color
- White to Almost white
- optical activity
- [α]20/D +6.7°, c = 2 in H2O
- InChI
- InChI=1/C7H15NO2.ClH/c1-4-10-7(9)6(8)5(2)3;/h5-6H,4,8H2,1-3H3;1H/t6-;/s3
- InChIKey
- PQGVTLQEKCJXKF-RGMNGODLSA-N
- SMILES
- [C@H](N)(C(C)C)C(=O)OCC.Cl |&1:0,r|
- CAS DataBase Reference
- 17609-47-1(CAS DataBase Reference)
MSDS
- Language:English Provider:Ethyl L-valinate hydrochloride
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
Ethyl L-valinate hydrochloride Usage And Synthesis
Chemical Properties
white crystalline powder
Uses
peptide synthesis
reaction suitability
reaction type: solution phase peptide synthesis
Synthesis
64-17-5
72-18-4
17609-47-1
The general procedure for the synthesis of L-valine ethyl ester hydrochloride from ethanol and L-valine is as follows: 5 kg (42.7 mol) of L-valine and 4 kg of anhydrous ethanol were added to a 50-liter glass reactor and stirred until complete dissolution. After cooling the reaction mixture to 0-10°C, 8.8 liters of thionyl chloride were added slowly and dropwise. After the dropwise addition was completed, the reaction mixture was gradually heated to reflux and the reaction was maintained for 18 hours. Upon completion of the reaction, the reaction solution was concentrated to dryness. Subsequently, 15 liters of isopropyl acetate was added to the dried residue at 15 to 20°C and stirred for 1 hour. Finally, the product was collected by diafiltration to give 6.1 kg of off-white solid, Intermediate 1 (where R1 is ethyl).
References
[1] Tetrahedron, 2005, vol. 61, # 35, p. 8423 - 8442
[2] Journal of the Indian Chemical Society, 2001, vol. 78, # 3, p. 137 - 141
[3] Journal of the American Chemical Society, 2018, vol. 140, # 22, p. 6818 - 6822
[4] Chemistry of Natural Compounds, 1994, vol. 30, # 2, p. 238 - 244
[5] Khimiya Prirodnykh Soedinenii, 1994, # 2, p. 261 - 268
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