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Ethyl 3-ethoxy-3-iminopropionate hydrochloride | CAS 2318-25-4

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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
Product Categories:
Mol File:2318-25-4.mol

Ethyl 3-ethoxy-3-iminopropionate hydrochloride Chemical Properties

Melting point 111-113 °C (decomp)
storage temp. 2-8°C
AppearanceWhite to off-white Solid
InChIInChI=1S/C7H13NO3.ClH/c1-3-10-6(8)5-7(9)11-4-2;/h8H,3-5H2,1-2H3;1H
InChIKeyHYMXUYQKXCHWDC-UHFFFAOYSA-N
SMILESC(OCC)(=O)CC(OCC)=N.[H]Cl
CAS DataBase Reference2318-25-4(CAS DataBase Reference)
EPA Substance Registry SystemEthyl 3-ethoxy-3-iminopropionate hydrochloride (2318-25-4)

Safety Information

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

MSDS Information

ProviderLanguage
SigmaAldrich English

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

Synthesis
Chemical PropertiesWhite crystalline powder

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 materialsEthyl cyanoacetate-->ethyl 3-ethoxy-3-iminopropionate-->Ethanol-->Hydrochloric acid-->Diethyl ether
Preparation ProductsCARBAMIMIDOYL-ACETIC ACID ETHYL ESTER-->3-Amino-3-iminopropanoic acid ethyl ester hydrochloride-->ETHYL 2-(5-CHLOROBENZO[D]OXAZOL-2-YL)ACETATE-->Ethyl (4-chloro-1,3-benzoxazol-2-yl)acetate

Declaration: The products displayed on this website are intended exclusively for industrial applications or scientific research. They are not intended for medical, pharmaceutical, or food use. In accordance with applicable laws and regulations, purchasing organizations must hold valid qualifications and approvals.

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