Basic information Safety Supplier Related

1-BENZYLPYRROLIDIN-3-YL-METHANOL

Basic information Safety Supplier Related

1-BENZYLPYRROLIDIN-3-YL-METHANOL Basic information

Product Name:
1-BENZYLPYRROLIDIN-3-YL-METHANOL
Synonyms:
  • 1-BENZYL-3-HYDROXYMETHYLPYRROLIDINE
  • 1-BENZYL-3-PYRROLIDIN-3-YLMETHANOL
  • CHEMBRDG-BB 4003810
  • 3-Pyrrolidinemethanol, 1-(phenylmethyl)-
  • 3-HYDROXYMETHYL-N-BENZYL- PYRROLIDINE
  • 1-BENZYL-DL-BETA-PROLINOL
  • 1-Benzyl-3-pyrrolidinemethanol
  • 1-(Phenylmethyl)-3-pyrrolidinemethanol
CAS:
5731-17-9
MF:
C12H17NO
MW:
191.27
Product Categories:
  • API intermediates
  • pharmacetical
  • Pyrrole&Pyrrolidine&Pyrroline
Mol File:
5731-17-9.mol
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1-BENZYLPYRROLIDIN-3-YL-METHANOL Chemical Properties

Boiling point:
129 °C(Press: 0.9 Torr)
Density 
1.082±0.06 g/cm3(Predicted)
storage temp. 
Store at room temperature
form 
solid
pka
14.93±0.10(Predicted)
Appearance
Light yellow to yellow Viscous liquid
InChI
InChI=1S/C12H17NO/c14-10-12-6-7-13(9-12)8-11-4-2-1-3-5-11/h1-5,12,14H,6-10H2
InChIKey
QPQQBJDSKDWQMJ-UHFFFAOYSA-N
SMILES
N1(CC2=CC=CC=C2)CCC(CO)C1
CAS DataBase Reference
5731-17-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,T
Risk Statements 
25
Safety Statements 
45
RIDADR 
UN 2811 6.1 / PGIII
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933998090
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1-BENZYLPYRROLIDIN-3-YL-METHANOL Usage And Synthesis

Synthesis

51535-00-3

5731-17-9

Example A: Synthesis of N-benzyl-3-hydroxymethylpyrrolidine Step a: Reduction of methyl 1-benzyl-5-oxopyrrolidine-3-carboxylate to 1-benzyl-3-hydroxymethylpyrrolidine Under an inert atmosphere, methyl 1-benzyl-5-oxopyrrolidine-3-carboxylate (1.0 equiv, commercially available) was dissolved in toluene and the mixture was cooled to 0 °C. To the cooled mixture was slowly added a dimethyl sulfide solution of borane-dimethyl sulfide complex (3.75 equiv.). The reaction mixture was heated to 100°C-110°C and refluxed for 16 hours. Upon completion of the reaction, the mixture was cooled to room temperature, further cooled to -5 °C to -10 °C, and then sodium bicarbonate solution was added dropwise. The mixture was slowly warmed to room temperature and then refluxed for 2 hours. After the reaction mixture was cooled, the organic layer was separated and the aqueous layer was extracted with toluene. The combined toluene layers were washed sequentially with water and brine. Finally, the organic solvent was removed by evaporation under reduced pressure to afford the target product N-benzyl-3-hydroxymethylpyrrolidine in 99.14% yield.

References

[1] Patent: WO2006/18708, 2006, A2. Location in patent: Page/Page column 21-22
[2] Letters in Organic Chemistry, 2011, vol. 8, # 3, p. 155 - 162
[3] Patent: US2004/147502, 2004, A1. Location in patent: Page/Page column 36-37
[4] Organic Letters, 1999, vol. 1, # 5, p. 799 - 801
[5] Patent: US2005/165005, 2005, A1. Location in patent: Page/Page column 59-60

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