| | Identification | More |  | [Name] 
 Ethyl 3-ethoxy-3-iminopropionate hydrochloride
 |  | [CAS] 
 2318-25-4
 |  | [Synonyms] 
 3-ETHOXY-3-IMINOPROPANOIC ACID ETHYL ESTER HYDROCHLORIDE
 3-ETHOXY-3-IMINOPROPIONIC ACID ETHYL ESTER HCL
 3-ETHOXY-3-IMINOPROPIONIC ACID ETHYL ESTER HYDROCHLORIDE
 AURORA KA-6317
 DIETHYL MALONMONOIMIDATE HYDROCHLORIDE
 ETHYL 3-ETHOXY-3-IMINOPROPIONATE HYDROCHLORIDE
 ETHYL-MONO-IMIDO-MALONATE HCL
 IMINOESTERCHLOROHYDRATE
 propanoicacid,3-ethoxy-3-imino-,ethylester,hydrochloride
 Ethyl3-ethoxy-3-iminopropionateHCl
 3-Ethoxy-3-Iminopropanoic Acid Ethyl Ester HCl
 Rthyl-Rthoxy-Iminopropionate Hydrochloride
 Ethyl 3-ethoxy-3-iminopropioate hydrochloride
 3-Ethoxy-3-iminopropionic acid ester ester hydrochloride
 ETHYLβ-ETHOXYL-β-IMIDO-PROPIONATEHYDROCHLORIDE
 ETHYL-(ETHYLAMIDIN)ACRYLATE HYDROCHLORIDE
 |  | [EINECS(EC#)] 
 219-028-1
 |  | [Molecular Formula] 
 C7H14ClNO3
 |  | [MDL Number] 
 MFCD00051405
 |  | [Molecular Weight] 
 195.64
 |  | [MOL File] 
 2318-25-4.mol
 | 
 | Safety Data | Back Directory |  | [Hazard Codes ] 
 Xi
 |  | [Risk Statements ] 
 R36/37/38:Irritating to eyes, respiratory system and skin .
 |  | [Safety Statements ] 
 S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
 |  | [WGK Germany ] 
 3
 
 |  | [F ] 
 10-21
 |  | [HS Code ] 
 29252900
 | 
 | Hazard Information | Back Directory |  | [Chemical Properties] 
 White crystalline powder
 |  | [Synthesis] 
 
 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
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