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2-(Aminomethyl)-1-ethylpyrrolidine

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2-(Aminomethyl)-1-ethylpyrrolidine Basic information

Product Name:
2-(Aminomethyl)-1-ethylpyrrolidine
Synonyms:
  • (1-Ethyl-2-pyrrolidinyl)methanamine
  • 1-Ethyl-2-(aminomethyl)pyrrolidine
  • 1-Ethyl-2-pyrrolidinemethylamine
  • 2-(Aminomethyl)-N-ethylpyrrolidine
  • AMisulpride IMpurity A (Sulpiride IMpurity A)
  • Sulpiride IMpurity A (AMisulpride IMpurity A)
  • Pyrrolidine, 2-(aminomethyl)-1-ethyl-
  • 2-(Aminomethyl)-1-ethylpyrrolidine 97%
CAS:
26116-12-1
MF:
C7H16N2
MW:
128.22
EINECS:
247-466-3
Product Categories:
  • Piperidines
  • API intermediates
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyrrolidines
  • john's
Mol File:
26116-12-1.mol
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2-(Aminomethyl)-1-ethylpyrrolidine Chemical Properties

Boiling point:
58-60 °C16 mm Hg(lit.)
Density 
0.884 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.4670(lit.)
Flash point:
135 °F
storage temp. 
2-8°C
solubility 
Chloroform (Sparingly), Methanol (Sparingly)
pka
10.04±0.40(Predicted)
form 
Liquid
color 
Clear yellow
InChI
InChI=1S/C7H16N2/c1-2-9-5-3-4-7(9)6-8/h7H,2-6,8H2,1H3
InChIKey
UNRBEYYLYRXYCG-UHFFFAOYSA-N
SMILES
N1(CC)CCCC1CN
LogP
0.433 (est)
CAS DataBase Reference
26116-12-1(CAS DataBase Reference)
NIST Chemistry Reference
2-Pyrrolidinemethanamine, 1-ethyl-(26116-12-1)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
26-36
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
HazardClass 
3.2
PackingGroup 
III
HS Code 
29339900

MSDS

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2-(Aminomethyl)-1-ethylpyrrolidine Usage And Synthesis

Chemical Properties

clear yellow liquid

Uses

2-(Aminomethyl)-1-ethylpyrrolidine is used as a reagent in the synthesis of S-Desethyl S-Methyl Amisulpride (D289595)

Synthesis

2167-14-8

26116-12-1

General procedure for the synthesis of N-ethyl-2-aminomethylpyrrolidine from 1-ethyl-1H-pyrrole-2-carboxaldehyde: 60 g of 1-ethyl-1H-pyrrole-2-carboxaldehyde was added to an autoclave, and 5 g of palladium-carbon catalyst at a mass percent concentration of 5% and 15 g of liquid ammonia were added to carry out hydrogenation and reductive amination reactions. The reaction conditions were hydrogen pressure of 35 kg and temperature of 95°C. After completion of the reaction, the system was cooled, the gas was expelled, and filtration was carried out. The filter cake was washed with methanol, and the filtrate and washings were combined to recover methanol. Finally, the target product N-ethyl-2-aminomethylpyrrole was obtained by purification via decompression distillation in a yield of 53.7 g and 86%. The reaction equation was as follows:

References

[1] Patent: CN107973735, 2018, A. Location in patent: Paragraph 0017; 0027-0029

2-(Aminomethyl)-1-ethylpyrrolidine Preparation Products And Raw materials

Preparation Products

Raw materials

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