1-PYRIDIN-3-YL-ETHYLAMINE
1-PYRIDIN-3-YL-ETHYLAMINE Basic information
- Product Name:
- 1-PYRIDIN-3-YL-ETHYLAMINE
- Synonyms:
-
- 3-(1-aminoethyl)pyridine
- alpha-methyl-3-pyridinemethylamin
- 1-(3-Pyridyl)ethylamine, 96%
- 3-Pyridinemethylamine, alpha-methyl-
- alpha-Methyl-3-pyridinemethylamine
- Brn 0110124
- 1-pyridin-3-ylethanamine (racemic-)
- 1-(3-pyridinyl)ethanamine
- CAS:
- 56129-55-6
- MF:
- C7H10N2
- MW:
- 122.17
- Mol File:
- 56129-55-6.mol
1-PYRIDIN-3-YL-ETHYLAMINE Chemical Properties
- Melting point:
- 63 °C
- Boiling point:
- 118-120 °C(Press: 14 Torr)
- Density
- 1.014 g/cm3(Temp: 25 °C)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 8.81±0.29(Predicted)
- form
- liquid
- color
- Colourless
- Sensitive
- Air Sensitive
- CAS DataBase Reference
- 56129-55-6(CAS DataBase Reference)
Safety Information
- Hazard Codes
- T,Xi
- Risk Statements
- 25-41-43-37/38
- Safety Statements
- 26-36/37/39-45-39
- RIDADR
- UN2735
- WGK Germany
- 3
- HazardClass
- 8
- PackingGroup
- III
- HS Code
- 2933399990
1-PYRIDIN-3-YL-ETHYLAMINE Usage And Synthesis
Uses
1-pyridin-3-ylethanamine is mainly used in scientific research experiments.
Synthesis
350-03-8
56129-55-6
General procedure for the synthesis of 1-(3-pyridyl)ethylamine from 3-acetylpyridine: 1. 3-Acetylpyridine (0.5 g, 4.1 mmol), potassium carbonate (1.7 g, 12.3 mmol), hydroxylamine hydrochloride (342 mg, 5 mmol), and methanol (10 mL) were mixed and the reaction was stirred for 16 hours at room temperature. 2. After completion of the reaction, the mixture was filtered and the filtrate was collected. 3. Zinc powder (1.3 g, 21 mmol) and ammonium chloride (1.1 g, 21 mmol) were added to the filtrate and stirring was continued at room temperature for 24 hours. 4. At the end of the reaction, water (10 mL) was added to the reaction mixture and filtered again. 5. The filtrate was concentrated and dried to give the white solid product 1-(3-pyridyl)ethylamine in 300 mg yield and 60% yield. Product characterization data: 1H NMR (300 MHz, DMSO-d6) δ 8.52 (d, J = 4.9 Hz, 1H), 8.32 (td, J = 7.7, 1.9 Hz, 1H), 7.68 (d, J = 7.7 Hz, 1H), 7.28 (ddd, J = 7.5, 4.9, 1.1 Hz, 1H), 4.6 (q, J = 6.0 Hz, 1H) , 1.25 (d, J = 6.6 Hz, 3H); MS (ESI) m/z 123.4 [M + 1]+.
References
[1] Patent: WO2008/51493, 2008, A2. Location in patent: Page/Page column 105
[2] Patent: WO2003/99776, 2003, A1. Location in patent: Page 94-95
[3] Journal of the American Chemical Society, 1944, vol. 66, p. 1293
[4] Patent: WO2006/110668, 2006, A1. Location in patent: Page/Page column 54
[5] Patent: WO2009/42694, 2009, A1. Location in patent: Page/Page column 66
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