2-(Aminomethyl)-1-ethylpyrrolidine
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
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)
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
- Language:English Provider:1-Ethylpyrrolidin-2-ylmethylamine
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
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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2-(Aminomethyl)-1-ethylpyrrolidine(26116-12-1)Related Product Information
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