Identification | Back Directory | [Name]
tert-butyl 2-(aminocarbonyl)pyrrolidine-1-carboxylate | [CAS]
54503-10-5 | [Synonyms]
Boc-DL-prolinaMide L-1-BOC-PROLINAMIDE N-Boc-D-Prolinamide 1-Boc-piperidine-2-carboxamide 1-Boc-2-(AMinocarbonyl)pyrrolidine tert-butyl 2-carbaMoylpyrrolidine-1-carboxylate 1-(tert-Butoxycarbonyl)piperidine-2-carboxamide tert-Butyl 2-carbamoyllpyrrolidine-1-carboxylate ert-butyl2-(aminocarbonyl)pyrrolidine-1-carboxylate tert-butyl 2-(aminocarbonyl)pyrrolidine-1-carboxylate tert-Butyl (R)-2-(aminocarbonyl)pyrrolidine-1-carboxylate 2-Methyl-2-propanyl (2R)-2-carbaMoyl-1-pyrrolidinecarboxylate 2-Aminocarbonyl-1-pyrrolidinecarboxylic acid 1,1-dimethylethyl ester 1-Pyrrolidinecarboxylic acid, 2-(aMinocarbonyl)-, 1,1-diMethylethyl ester | [EINECS(EC#)]
259-189-5 | [Molecular Formula]
C10H18N2O3 | [MDL Number]
MFCD02183582 | [MOL File]
54503-10-5.mol | [Molecular Weight]
214.26 |
Chemical Properties | Back Directory | [Boiling point ]
370.1±31.0 °C(Predicted) | [density ]
1.155±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
15.97±0.20(Predicted) | [Appearance]
White to off-white Solid | [Optical Rotation]
Consistent with structure |
Hazard Information | Back Directory | [Synthesis]
GENERAL METHOD: 20 g (93 mmol) of Boc-L-proline was dissolved in 150 mL of anhydrous acetonitrile, and 19.5 g (120 mmol) of 1,1'-carbonyldiimidazole, 21.0 mL (150 mmol) of trimethylamine, and 19.2 g (200 mmol) of ammonium carbonate were added sequentially. The reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, the mixture was poured into 250 mL of saturated potassium carbonate solution and extracted with dichloromethane (3 x 250 mL). The organic phases were combined, washed twice with 150 mL of water and dried over sodium sulfate. After removing the solvent under reduced pressure, the crude product was purified by rapid chromatography on silica gel with the eluent being ethylhexane-ethyl acetate (100:0→1:1). The product was obtained as 12.3 g in 62% yield. MS data: m/z (Irel, %) 215.1 (100) [M + H]+. | [References]
[1] Russian Journal of General Chemistry, 2017, vol. 87, # 4, p. 717 - 730 [2] Zh. Obshch. Khim., 2017, vol. 87, # 4, p. 584 - 596,13 [3] Synthetic Communications, 2007, vol. 37, # 21, p. 3793 - 3799 [4] Journal of Medicinal Chemistry, 2007, vol. 50, # 9, p. 2225 - 2239 [5] Tetrahedron, 2008, vol. 64, # 12, p. 2801 - 2815 |
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