Basic information Safety Supplier Related

(S)-1-N-Boc-2-(aminomethyl)pyrrolidine

Basic information Safety Supplier Related

(S)-1-N-Boc-2-(aminomethyl)pyrrolidine Basic information

Product Name:
(S)-1-N-Boc-2-(aminomethyl)pyrrolidine
Synonyms:
  • tert-Butyl 2-(1-aminoethyl)-1-pyrrolidinecarboxylate
  • (S)-TERT-BUTYL-2-(AMINOMETHYL)PYRROLIDINE-1-CARBOXYLATE
  • RARECHEM AL BW 2320
  • (S)-2-AMINOMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
  • (S)-2-(AMINOMETHYL)-1-N-BOC-PYRROLIDINE
  • (S)-2-AMINOMETHYL-1-BOC-PYRROLIDINE
  • (S)-1-BOC-2-(AMINOMETHYL)PYRROLIDINE
  • (S)-1-N-Boc-2-(aminomethyl)pyrrolidine
CAS:
119020-01-8
MF:
C10H20N2O2
MW:
200.28
EINECS:
251-228-4
Product Categories:
  • pharmacetical
  • Pyrrole&Pyrrolidine&Pyrroline
Mol File:
119020-01-8.mol
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(S)-1-N-Boc-2-(aminomethyl)pyrrolidine Chemical Properties

Boiling point:
98-112℃/1mm
Density 
1.044±0.06 g/cm3(Predicted)
refractive index 
1.4670-1.4710
storage temp. 
2-8°C
solubility 
Miscible with N-methylpyrrolidinone.
pka
9.91±0.29(Predicted)
form 
clear liquid
color 
Colorless to Almost colorless
BRN 
8905233
CAS DataBase Reference
119020-01-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,N,C
Risk Statements 
36/37/38-51/53-34-22
Safety Statements 
26-36/37/39-61-45
RIDADR 
3259
WGK Germany 
3
HazardClass 
8
PackingGroup 
HS Code 
29339900
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(S)-1-N-Boc-2-(aminomethyl)pyrrolidine Usage And Synthesis

Chemical Properties

Solid

Uses

(S)-2-Aminomethyl-1-Boc-pyrrolidine acts as an intermediate in organic synthesis. It is also used as a chiral and heterocyclic building block in synthetic chemistry.

Synthesis

168049-26-1

119020-01-8

GENERAL METHOD: Under stirring conditions, azide derivatives 9a or 9b (4.03 mmol) were dissolved in THF (1 mL), followed by the addition of solid triphenylphosphine (Ph3P, 4.03 mmol) and water (H2O, 6.04 mmol). The reaction mixture was stirred continuously for 12 h at room temperature. After completion of the reaction, the solvent was removed by concentration under reduced pressure. The crude product was purified by rapid column chromatography on silica gel with an eluent ratio of methanol-dichloromethane (9:1).

References

[1] Synthesis, 2005, # 14, p. 2407 - 2413
[2] Angewandte Chemie - International Edition, 2011, vol. 50, # 48, p. 11382 - 11385
[3] Synthetic Communications, 2011, vol. 41, # 17, p. 2517 - 2523
[4] Tetrahedron Letters, 2010, vol. 51, # 40, p. 5281 - 5286
[5] Phosphorus, Sulfur and Silicon and the Related Elements, 2013, vol. 188, # 4, p. 509 - 511

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