3-PROPYLPYRIDINE
3-PROPYLPYRIDINE Basic information
- Product Name:
- 3-PROPYLPYRIDINE
- Synonyms:
-
- 1-(3-Pyridyl)propane
- 3-propyl-pyridin
- Pyridine, 5-propyl
- 3-N-PROPYL PYRIDINE
- 3-PROPYLPYRIDINE
- Pyridine, 3-propyl-
- Einecs 225-122-3
- CAS:
- 4673-31-8
- MF:
- C8H11N
- MW:
- 121.18
- EINECS:
- 225-122-3
- Mol File:
- 4673-31-8.mol
3-PROPYLPYRIDINE Chemical Properties
- Melting point:
- 163 °C
- Boiling point:
- 75-77 °C(Press: 16 Torr)
- Density
- 0.9264 g/cm3
- storage temp.
- Inert atmosphere,Room Temperature
- pka
- 5.56±0.10(Predicted)
- Odor
- at 0.10 % in propylene glycol. sweet musty beany earthy woody
- Appearance
- Colorless to light yellow Liquid
- Odor Type
- beany
- LogP
- 2.359 (est)
- EPA Substance Registry System
- 3-Propylpyridine (4673-31-8)
3-PROPYLPYRIDINE Usage And Synthesis
Synthesis
75-03-6
4673-31-8
The general procedure for the synthesis of 3-propylpyridine from ethyl iodide was as follows: i) n-butyllithium (BuLi, 1.6 M hexane solution, 15.4 mL, 25 mmol) was added drop-wise to a tetrahydrofuran (THF, 35 mL) solution of diisopropylamine (3.53 mL, 24.7 mmol) at 0 °C. After 30 min, hexamethylphosphorotriamine (HMPA , 15.7 g, 24.7 mmol) was added and the mixture was kept at 0 °C for 15 min. Subsequently, a THF (10 mL) solution of 3-methylpyridine (2.3 g, 24.7 mmol) was added dropwise.After 30 min, a THF (10 mL) solution of ethyl iodide (EtI, 3.45 g, 24.7 mmol) was added dropwise.The reaction mixture was stirred for 1 h at room temperature. After completion of the reaction, the mixture was poured into 10% hydrochloric acid (HCl) solution. The aqueous phase was extracted with ether (Et2O), the organic phase was washed with water, dried over anhydrous sodium sulfate and concentrated under vacuum to give a yellow oily product (300 mg, 10% yield), which could be used in subsequent steps without further purification.
References
[1] Patent: WO2007/71358, 2007, A1. Location in patent: Page/Page column 32-33
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