Basic information Safety Supplier Related

tert-Butyl 3-aminopyrrolidine-1-carboxylate

Basic information Safety Supplier Related

tert-Butyl 3-aminopyrrolidine-1-carboxylate Basic information

Product Name:
tert-Butyl 3-aminopyrrolidine-1-carboxylate
Synonyms:
  • TERT-BUTYL 3-AMINOPYRROLIDINE-1-CARBOXYLATE
  • 1-BOC-3-AMINOPYRROLIDINE
  • 1-N-BOC-3-AMINO-PYRROLIDINE
  • (+/-)-3-AMINO-1-BOC-PYRROLIDINE
  • 3-AMINO-1-BOC-PYRROLIDINE
  • 3-AMINO-1-N-BOC-PYRROLIDINE
  • 3-AMINOPYRROLIDINE, N1-BOC PROTECTED
  • 3-AMINO-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
CAS:
186550-13-0
MF:
C9H18N2O2
MW:
186.25
EINECS:
624-257-9
Product Categories:
  • pharmacetical
  • Amines
  • Pyrrolidines
  • Pyrrole&Pyrrolidine&Pyrroline
Mol File:
186550-13-0.mol
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tert-Butyl 3-aminopyrrolidine-1-carboxylate Chemical Properties

Boiling point:
257.4±33.0 °C(Predicted)
Density 
1.022
Flash point:
91°C
refractive index 
1.4710
storage temp. 
2-8°C
pka
9.55±0.20(Predicted)
form 
powder to lump to clear liquid
color 
White or Colorless to Light yellow
Sensitive 
Air Sensitive
CAS DataBase Reference
186550-13-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,Xi,Xn
Risk Statements 
36/37/38-44-41-22
Safety Statements 
26-36/37/39
RIDADR 
2810
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
8
PackingGroup 
HS Code 
29339900
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tert-Butyl 3-aminopyrrolidine-1-carboxylate Usage And Synthesis

Chemical Properties

Colorless low melting solid or liquid

Uses

1-Boc-3-Aminopyrrolidine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Synthesis

862906-31-8

186550-13-0

Step (ii): preparation of tert-butyl 3-aminopyrrolidine-1-carboxylate (Formula 49) To a stirred solution of tert-butyl 3-hydroxypyrrolidine-1-carboxylate (Formula 48, 1.15 g, 4.16 mmol) in methanol (16.6 mL) was added 10% palladium/carbon catalyst (345 mg). The reaction mixture was stirred for 16 hours under a hydrogen atmosphere (hydrogen pressure applied via a double-layer balloon). Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad to remove the catalyst and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel fast column chromatography to afford the target compound tert-butyl 3-aminopyrrolidine-1-carboxylate (Formula 49, 640 mg) in 82% yield. 1H-NMR (CDCl3): δ 3.65-3.45 (m, 3H), 3.45-3.33 (m, 1H), 3.20-3.0 (m, 1H), 2.12-2.02 (m, 1H), 1.80-1.65 (m, 1H), 1.46 (s, 9H). Mass spectrum (m/z): 187 [M+H]+.

References

[1] Patent: WO2005/77924, 2005, A1. Location in patent: Page/Page column 76
[2] Patent: WO2011/30349, 2011, A1. Location in patent: Page/Page column 36-37

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