2-[(Acetylthio)methyl]-phenylpropionic acid
2-[(Acetylthio)methyl]-phenylpropionic acid Basic information
- Product Name:
- 2-[(Acetylthio)methyl]-phenylpropionic acid
- Synonyms:
-
- 2-[(Acetylthio)methyl]-phenylpropionic acid
- 2-[(ACETYLETHIO)METHYL]PHENYLPROPIONIC ACID
- 2-[(Acetylthio)methyl]-3-phenylpropanoic acid 96%
- 3-(Acetylsulphanyl)-2-benzylpropanoic acid
- α-[(Acetylthio)Methyl]benzenepropanoic Acid
- 2-[(ACETYLTHIO)METHYL]-3-PHENYLPROPIONIC ACIDE
- 2-(Acetylthiomethyl)-3-phenylpropionic Acid
- 2-[(Acetylsulfanyl)methyl]-3-phenylpropionic Acid
- CAS:
- 91702-98-6
- MF:
- C12H14O3S
- MW:
- 238.3
- Product Categories:
-
- Aromatics
- Intermediates
- Sulfur & Selenium Compounds
- (intermediate of racecodotril)
- Mol File:
- 91702-98-6.mol
2-[(Acetylthio)methyl]-phenylpropionic acid Chemical Properties
- Melting point:
- 39 °C
- Boiling point:
- 381.9±35.0 °C(Predicted)
- Density
- 1.226±0.06 g/cm3(Predicted)
- refractive index
- 1.55
- storage temp.
- 2-8°C(protect from light)
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- powder to lump to clear liquid
- pka
- 4.06±0.10(Predicted)
- color
- White or Colorless to Yellow
- CAS DataBase Reference
- 91702-98-6
2-[(Acetylthio)methyl]-phenylpropionic acid Usage And Synthesis
Chemical Properties
Brownish Liquid
Uses
2-[(Acetylthio)methyl]-phenylpropionic acid is a racecadotril intermediate. It is also a β-thiopropionyl-amino acid derivative used as β-lactamase inhibitor.
Synthesis
5669-19-2
507-09-5
91702-98-6
General procedure for the synthesis of 3-(acetylthio)-2-benzylpropionic acid from 2-benzylpropenoic acid and thioacetic acid: 16.2 g of 2-benzylpropenoic acid and 12.3 mL of thioacetic acid were added to a clean and dry round-bottomed flask, and the reaction was stirred for 1 hour at 30 °C. Subsequently, the reaction mixture was warmed up to 60 °C and the stirring reaction was continued for 4 hours. Upon completion of the reaction, the excess thioacetic acid was removed by distillation to give the crude product of 3-(acetylthio)-2-benzylpropionic acid. Yield: 23.8 g.
References
[1] Journal of Medicinal Chemistry, 1994, vol. 37, # 15, p. 2461 - 2476
[2] Journal of Organic Chemistry, 2009, vol. 74, # 9, p. 3389 - 3393
[3] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 20, p. 5614 - 5619
[4] Journal of Medicinal Chemistry, 1992, vol. 35, # 3, p. 602 - 608
[5] Magnetic Resonance in Chemistry, 2000, vol. 38, # 6, p. 468 - 471
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