Basic information Safety Supplier Related

1-(3-CHLOROPROPYL)-PYRROLIDINE

Basic information Safety Supplier Related

1-(3-CHLOROPROPYL)-PYRROLIDINE Basic information

Product Name:
1-(3-CHLOROPROPYL)-PYRROLIDINE
Synonyms:
  • N-CHLOROPROPYL PYRROLIDINE
  • Pyrrolidine,1-(3-chloropropyl)-
  • Albb-007086
  • (3-Chloropropyl)pyrrolidine, HCl
  • 1-(3-CHLOROPROPYL)-PYRROLIDINE
CAS:
39743-20-9
MF:
C7H14ClN
MW:
147.65
Mol File:
39743-20-9.mol
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1-(3-CHLOROPROPYL)-PYRROLIDINE Chemical Properties

Boiling point:
88-89 °C(Press: 22 Torr)
Density 
1.016±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
pka
10.10±0.20(Predicted)
Appearance
Colorless to light yellow Liquid
InChI
InChI=1S/C7H14ClN/c8-4-3-7-9-5-1-2-6-9/h1-7H2
InChIKey
SPRTXTPFQKHSBG-UHFFFAOYSA-N
SMILES
N1(CCCCl)CCCC1
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Safety Information

HazardClass 
IRRITANT
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1-(3-CHLOROPROPYL)-PYRROLIDINE Usage And Synthesis

Synthesis

123-75-1

109-70-6

39743-20-9

Example 4 Synthesis of 1-(3-chloropropyl)pyrrolidine At 0°C, 186 g (1.18 mol) of 1-bromo-3-chloropropane was dissolved in 200 ml of ether and 2 equivalents of pyrrolidine were slowly added. After addition, the reaction mixture was gradually warmed to room temperature and stirred overnight. Upon completion of the reaction, the resulting white solid was removed by filtration. Ice-cold 10% hydrochloric acid solution was added to the filtrate and the ether layer was discarded after partitioning. The aqueous phase was alkalized with ice-cold 20% sodium hydroxide solution and subsequently extracted with ether. The organic phases were combined and dried over anhydrous sodium sulfate. The ether was evaporated under reduced pressure and the residue was distilled under reduced pressure at 95 °C/30 mmHg to give 91 g of the target product 1-(3-chloropropyl)pyrrolidine as a pale yellow liquid in 53% yield.

References

[1] Pharmazie, 1980, vol. 35, # 2, p. 69 - 72
[2] Patent: EP1593679, 2005, A1. Location in patent: Page/Page column 27
[3] Patent: US2005/245524, 2005, A1. Location in patent: Page/Page column 27
[4] European Journal of Medicinal Chemistry, 2014, vol. 89, p. 198 - 206
[5] Journal of the American Chemical Society, 1955, vol. 77, p. 2855,2857

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