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2213-08-3

2213-08-3 Structure

2213-08-3 Structure
IdentificationBack Directory
[Name]

ETHYL 3-(N-METHYLAMINO) PROPIONATE
[CAS]

2213-08-3
[Synonyms]

114537
Ethyl N-Methyl-β-alaninate
Ethyl N-methyl-beta-alaninate
N-Methyl-b-alanine ethyl ester
Ethyl 3-(MethylaMino)propanoate
ethyl N-methyl-2-aminopropionate
β-Alanine, N-methyl-, ethyl ester
ETHYL 3-(N-METHYLAMINO) PROPIONATE
.beta.-Alanine, N-methyl-, ethyl ester
3-methylaminopropanoic acid ethyl ester
3-methylaminopropionic acid ethyl ester
3-(Methylamino)propionic acid ethyl ester
[Molecular Formula]

C6H13NO2
[MDL Number]

MFCD00672194
[MOL File]

2213-08-3.mol
[Molecular Weight]

131.18
Chemical PropertiesBack Directory
[Boiling point ]

242.49°C (rough estimate)
[density ]

1.0070
[refractive index ]

1.4443 (estimate)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[solubility ]

Chloroform (Sparingly), Ethyl Acetate (Slightly)
[form ]

Oil
[pka]

9.55±0.10(Predicted)
[color ]

Colourless
[InChI]

InChI=1S/C6H13NO2/c1-3-9-6(8)4-5-7-2/h7H,3-5H2,1-2H3
[InChIKey]

XVIJMHJTEHBUJI-UHFFFAOYSA-N
[SMILES]

C(=O)(OCC)CCNC
Safety DataBack Directory
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[HS Code ]

2922498590
Hazard InformationBack Directory
[Uses]

Ethyl N-Methyl-beta-alaninate is an intermediate in the synthesis of Tolafentrine (T531000), which is a dual-selective phosphodiesterase 3/4 inhibitor used in chronic experimental pulmonary hypertension.
[Synthesis Reference(s)]

Journal of the American Chemical Society, 71, p. 2124, 1949 DOI: 10.1021/ja01174a061
[Synthesis]

Methylamine

74-89-5

Ethyl acrylate

140-88-5

ETHYL 3-(N-METHYLAMINO) PROPIONATE

2213-08-3

1. cool 33% methylamine ethanol solution (100 mL, 805 mmol) in an ice bath at 0 °C. 2. Ethyl acrylate (11.0 mL, 10.1 g, 101 mmol) was added slowly, keeping the reaction temperature at 0 °C with continuous stirring for 2 hours. 3. Gradually warm the reaction mixture to room temperature and continue stirring for 15 minutes. 4. All volatiles were removed by distillation under reduced pressure. 5. The resulting residue (ethyl 3-(methylamino)propionate crude, 11.2 g) was used directly in the subsequent reaction without further purification.

[References]

[1] Monatshefte fur Chemie, 2011, vol. 142, # 10, p. 1055 - 1059
[2] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1980, p. 1739 - 1745
[3] Journal of Heterocyclic Chemistry, 1997, vol. 34, # 1, p. 87 - 91
[4] Liebigs Annalen der Chemie, 1980, # 9, p. 1438 - 1447
[5] Journal of the American Chemical Society, 1949, vol. 71, p. 2129
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