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Ethyl 3-ethoxy-3-iminopropionate hydrochloride

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Ethyl 3-ethoxy-3-iminopropionate hydrochloride Basic information

Product Name:
Ethyl 3-ethoxy-3-iminopropionate hydrochloride
Synonyms:
  • propanoicacid,3-ethoxy-3-imino-,ethylester,hydrochloride
  • 3-ethoxy-3-iminopropionate hydrochL
  • 3-ETHOXY-3-IMINOPROPANOIC ACID ETHYL ESTER HYDROCHLORIDE
  • 3-ETHOXY-3-IMINOPROPIONIC ACID ETHYL ESTER HCL
  • 3-ETHOXY-3-IMINOPROPIONIC ACID ETHYL ESTER HYDROCHLORIDE
  • DIETHYL MALONMONOIMIDATE HYDROCHLORIDE
  • IMINOESTERCHLOROHYDRATE
  • ETHYL 3-ETHOXY-3-IMINOPROPIONATE HYDROCHLORIDE
CAS:
2318-25-4
MF:
C7H13NO3.ClH
MW:
195.64
EINECS:
219-028-1
Mol File:
2318-25-4.mol
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Ethyl 3-ethoxy-3-iminopropionate hydrochloride Chemical Properties

Melting point:
111-113 °C (decomp)
storage temp. 
2-8°C
Appearance
White to off-white Solid
InChI
InChI=1S/C7H13NO3.ClH/c1-3-10-6(8)5-7(9)11-4-2;/h8H,3-5H2,1-2H3;1H
InChIKey
HYMXUYQKXCHWDC-UHFFFAOYSA-N
SMILES
C(OCC)(=O)CC(OCC)=N.[H]Cl
CAS DataBase Reference
2318-25-4(CAS DataBase Reference)
EPA Substance Registry System
Ethyl 3-ethoxy-3-iminopropionate hydrochloride (2318-25-4)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
10-21
HS Code 
29252900

MSDS

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Ethyl 3-ethoxy-3-iminopropionate hydrochloride Usage And Synthesis

Chemical Properties

White crystalline powder

Synthesis

64-17-5

105-56-6

2318-25-4

Ethyl cyanoacetate (30 mL, 281 mmol) was dissolved with anhydrous ethanol (18.1 mL, 278 mmol) in anhydrous ether (28.1 mL) at 0°C and stirred to form a homogeneous solution. Dry hydrogen chloride gas was passed into the solution until saturation. Subsequently, the reaction mixture was warmed up to 22°C with continuous stirring for 20 hours. Upon completion of the reaction, the solvent was removed by concentration under reduced pressure to afford ethyl 3-ethoxy-3-iminopropionate hydrochloride (54.4 g, 99% yield). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 4.73 (q, J = 7.1 Hz, 2H); 4.24 (q, J = 7.2 Hz, 2H); 3.89 (s, 2H); 1.51 (t, J = 7.0 Hz, 3H); 1.30 (t, J = 7.2 Hz, 3H) ppm.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 23, p. 7207 - 7213
[2] Chemical and Pharmaceutical Bulletin, 1985, vol. 33, # 7, p. 3046 - 3049
[3] Heterocycles, 1996, vol. 43, # 9, p. 1981 - 1989
[4] Tetrahedron, 2009, vol. 65, # 4, p. 757 - 764
[5] Patent: WO2006/7700, 2006, A1. Location in patent: Page/Page column 66-67

Ethyl 3-ethoxy-3-iminopropionate hydrochloride Preparation Products And Raw materials

Raw materials

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