R-N-BENZYL-PROLINE
R-N-BENZYL-PROLINE Basic information
- Product Name:
- R-N-BENZYL-PROLINE
- Synonyms:
-
- R-N-BENZYL-PROLINE
- N-Benzyl-D-proline
- (2R)-1-benzylpyrrolidine-2-carboxylic acid
- 1-Benzyl-D-proline
- D-Proline, 1-(phenylmethyl)-
- benzyl-D-proline
- CAS:
- 56080-99-0
- MF:
- C12H15NO2
- MW:
- 205.25
- Mol File:
- 56080-99-0.mol
R-N-BENZYL-PROLINE Chemical Properties
- Boiling point:
- 343.1±35.0 °C(Predicted)
- Density
- 1.205±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 2.35±0.20(Predicted)
- form
- solid
- color
- White to light yellow
- optical activity
- 31.9°(C=1.00g/100ml MEOH)
R-N-BENZYL-PROLINE Usage And Synthesis
Uses
(R)-1-Benzylpyrrolidine-2-carboxylic acid is a proline derivative[1].
Synthesis
100-44-7
344-25-2
56080-99-0
General procedure for the synthesis of N-benzyl-D-proline from benzyl chloride and D-proline: a suspension of D-proline (115 g, 1 mol), potassium hydroxide (168.3 g, 3 mol) and isopropanol (1 L) was stirred at 40°C until the suspension became clear. Subsequently, benzyl chloride (137.3 g, 1.1 mol) was slowly added and stirring was continued at 40°C for 6 hours. Upon completion of the reaction, the reaction mixture was cooled to 0-5°C and the pH was adjusted to 5-6 with concentrated hydrochloric acid (145 mL). the reaction mixture was diluted with chloroform (3 L) and stirred for 18 h. The reaction was purified by filtration. The resulting KCl was removed by filtration, the filtrate was concentrated and the crude product was recrystallized from acetone to give N-benzyl-D-proline in 79% yield (161.8 g). [39] The product was characterized as follows: 1H-NMR (CDCl3, ppm): δ 7.2-7.4 (m, 5H), 4.0-4.4 (dd, 2H), 3.8 (dd, 1H), 3.6-3.7 (m, 1H), 2.8 (dd, 1H), 1.8-2.4 (m, 4H). [40] Specific optical rotation [α]D25 = +28.4 (c = 1, EtOH). [41] Melting point 174-175°C.
References
[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. DOI:10.1080/10408398.2012.708368
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