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3-Amino-3-(4-methylphenyl)propionic acid

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3-Amino-3-(4-methylphenyl)propionic acid Basic information

Product Name:
3-Amino-3-(4-methylphenyl)propionic acid
Synonyms:
  • 3-AMINO-3-(P-TOLYL)PROPIONIC ACID 98%
  • 3-Amino-3-(p-tolyl)propionic acid,98%
  • 3-AMINO-3-(4-METHYLPHENYL)PROPANOIC ACID
  • 3-AMINO-3-(4-METHYLPHENYL)PROPIONIC ACID
  • 3-AMINO-3-(P-TOLYL)PROPIONIC ACID
  • RARECHEM AK HC T309
  • Benzenepropanoic acid, .beta.-amino-4-methyl-
  • 3-Amino-3-(p-tolyl)propionic Acid
CAS:
68208-18-4
MF:
C10H13NO2
MW:
179.22
Product Categories:
  • B-Amino
  • C10
  • Carbonyl Compounds
  • Carboxylic Acids
Mol File:
68208-18-4.mol
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3-Amino-3-(4-methylphenyl)propionic acid Chemical Properties

Melting point:
219 °C (dec.)(lit.)
Boiling point:
311.75°C (rough estimate)
Density 
1.1248 (rough estimate)
refractive index 
1.4989 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
3.71±0.10(Predicted)
Appearance
White to off-white Solid
CAS DataBase Reference
68208-18-4(CAS DataBase Reference)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29224999

MSDS

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3-Amino-3-(4-methylphenyl)propionic acid Usage And Synthesis

Chemical Properties

white to off-white granular or crystalline powder

Synthesis

141-82-2

104-87-0

68208-18-4

To a 250 mL round bottom flask was added 50.0 g (0.42 mol) of p-toluylaldehyde, 47.6 g (0.46 mol) of malonic acid and 64.2 g (0.83 mol) of ammonium acetate dissolved in ethanol. The reaction mixture was heated to 80-90°C under stirring and refluxed for 7.5 hours. Upon completion of the reaction, the mixture was cooled to 0-5°C and stirred for 30 min, followed by filtration to afford 51.4 g of 3-amino-3-(p-tolyl)propionic acid (racemic mixture) as a white powder (68.9% isolated yield based on p-toluylaldehyde). The physical properties of 3-amino-3-(p-tolyl)propionic acid (racemic mixture) are as follows: 1H-NMR (δ, ppm, D2O + DCl): 2.30 (s, 3H), 3.04 (dd, 1H, J = 17.1, 6.8 Hz), 3.20 (dd, 1H, J = 17.1, 7.3 Hz), 4.74 (dd, 1H, J = 7.3, 6.8 Hz), 7.29 (d, 2H, J = 8.3 Hz), 7.36 (d, 2H, J = 8.3 Hz). 13C-NMR (δ, ppm, D2O + DCl): 23.4, 40.7, 54.4, 130.0, 133.0, 135.0, 143.1, 176.3. MS (EI) m/z: 179 (M+). MS (CI, i-C4H10) m/z: 180 (MH+). Elemental analysis: Calculated C, 67.02%; H, 7.31%; N, 7.82%. Measured values C, 67.05%; H, 7.40%; N, 7.66%.

References

[1] Patent: EP1621529, 2006, A1. Location in patent: Page/Page column 27-28
[2] European Journal of Medicinal Chemistry, 2018, vol. 156, p. 252 - 268
[3] Advanced Synthesis and Catalysis, 2010, vol. 352, # 2-3, p. 395 - 406
[4] ACS Medicinal Chemistry Letters, 2014, vol. 5, # 11, p. 1207 - 1212
[5] Bulletin de la Societe Chimique de France, 1987, # 6, p. 1079 - 1083

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