Basic information Safety Supplier Related

1-BENZYL-3-(TERT-BUTOXYCARBONYLAMINO)PYRROLIDINE

Basic information Safety Supplier Related

1-BENZYL-3-(TERT-BUTOXYCARBONYLAMINO)PYRROLIDINE Basic information

Product Name:
1-BENZYL-3-(TERT-BUTOXYCARBONYLAMINO)PYRROLIDINE
Synonyms:
  • 1-BENZYL-3-(TERT-BUTOXYCARBONYLAMINO)PYRROLIDINE
  • (R)-1-Benzyl-3-(Boc-amino)pyrrolidine
  • Carbamic acid,N-[1-(phenylmethyl)-3-pyrrolidinyl]-, 1,1-dimethylethyl ester
  • tert-Butyl N-(1-benzylpyrrolidin-3-yl)carbamate
  • N-benzyl-3-(R)-((1,1-dimethylethoxycarbonyl)amino)pyrrolidine
  • N-[1-(phenylmethyl)-3-pyrrolidinyl]carbamic acid tert-butyl ester
  • 1-Benzyl-3-(tert-butoxycarbonylamino)pyrrolidine >
CAS:
99735-30-5
MF:
C16H24N2O2
MW:
276.37
Product Categories:
  • 3-Aminopyrrolidines
  • 3-Aminopyrrolidines (Racemic)
Mol File:
99735-30-5.mol
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1-BENZYL-3-(TERT-BUTOXYCARBONYLAMINO)PYRROLIDINE Chemical Properties

Melting point:
113 °C
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
color 
White to Almost white
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Safety Information

HS Code 
9999999999
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1-BENZYL-3-(TERT-BUTOXYCARBONYLAMINO)PYRROLIDINE Usage And Synthesis

Synthesis

24424-99-5

18471-40-4

99735-30-5

General procedure for the synthesis of 1-benzyl-3-(Boc-amino)pyrrolidine from di-tert-butyl dicarbonate and 1-benzylpyrrolidin-3-amine: 1-benzylpyrrolidin-3-amine (10 g, 57 mmol) was dissolved in 3M aqueous sodium hydroxide (21 ml) and tertiary butyl alcohol (114 ml) in a 500 ml reaction vessel. Di-tert-butyl dicarbonate (Boc2O; 13.07 g, 59.9 mmol) was slowly added to the above solution under stirring conditions. The reaction mixture was stirred at room temperature for 12 hours. After completion of the reaction, the reaction mixture was extracted with ethyl acetate (2×). The organic layers were combined and washed sequentially with 0.1 N hydrochloric acid solution and saturated brine, then dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The crude product obtained was purified by silica gel column chromatography to afford 15.25 g of 1-benzyl-3-(Boc-amino)pyrrolidine as a white solid (97% yield). The structure of the product was confirmed by 1H-NMR (200 MHz, CDCl3) and LC/MS (M+H: 277).

References

[1] Patent: WO2008/54154, 2008, A1. Location in patent: Page/Page column 76; 80-81; 162-163; 168
[2] Patent: WO2007/52938, 2007, A1. Location in patent: Page/Page column 22-23

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