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3,5-Diethyl-1,2-dihydro-1-phenyl-2-propylpyridine

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3,5-Diethyl-1,2-dihydro-1-phenyl-2-propylpyridine Basic information

Product Name:
3,5-Diethyl-1,2-dihydro-1-phenyl-2-propylpyridine
Synonyms:
  • 3,5-DIETHYL-1,2-DIHYDRO-1-PHENYL-2-PROPYLPYRIDINE
  • 1-Phenyl-3,5-diethyl-2-propyl-1,2-dihydropyridine
  • 3,5-diethyl-1,2-dihydro-1-phenyl-2-propyl-pyridin
  • Pyridine, 3,5-diethyl-1,2-dihydro-1-phenyl-2-propyl-
  • 3,5-DIETHYL-1-PHENYL-2-PROPYL-1,2-DIHYDROPYRIDINE
  • 3,5-Diethyl-1,2-dihydro-1-phen
  • 3,5-Diethyl-1,2-dihydro-1-phenyl-2-n-propylpyridine, tech. 75%
  • 3,5-diethyl-1-phenyl-2-propyl-2H-pyridine
CAS:
34562-31-7
MF:
C18H25N
MW:
255.4
EINECS:
252-091-3
Mol File:
34562-31-7.mol
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3,5-Diethyl-1,2-dihydro-1-phenyl-2-propylpyridine Chemical Properties

Boiling point:
125℃/0.5mm
Density 
0.97
vapor pressure 
0.003Pa at 25℃
Flash point:
>148 °C
refractive index 
1.5675
storage temp. 
2-8°C
pka
0.85±0.70(Predicted)
Water Solubility 
53.23μg/L at 25℃
InChI
InChI=1S/C18H25N/c1-4-10-18-16(6-3)13-15(5-2)14-19(18)17-11-8-7-9-12-17/h7-9,11-14,18H,4-6,10H2,1-3H3
InChIKey
IAAASXBHFUJLHW-UHFFFAOYSA-N
SMILES
C1(CCC)N(C2=CC=CC=C2)C=C(CC)C=C1CC
LogP
6.5 at 20℃
EPA Substance Registry System
3,5-Diethyl-1,2-dihydro-1-phenyl-2-propylpyridine (34562-31-7)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
21/22-36/38
Safety Statements 
26
TSCA 
Yes
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3,5-Diethyl-1,2-dihydro-1-phenyl-2-propylpyridine Usage And Synthesis

Uses

3,5-diethyl-1,2-dihydro-1-phenyl-2-propylpyridine (DHP) is the main active ingredient resulting from the condensation reaction of butyraldehyde and aniline. It is a useful research chemical.

Preparation

3,5-diethyl-1,2-dihydro-1-phenyl-2-propylpyridine (DHP) was prepared using methods shown below. A 1000 mL four neck flask was equipped with a mechanical stirrer, a reflux condenser, a thermometer, and an addition funnel. An ice-water bath was used to cool the flask as needed. The flask was charged with 86 g de-ionized water, 9.8 g (0.16 mole) acetic acid, and 216 g (3.0 mol) butyraldehyde. With cooling and stirring, 60 g (0.64 mole) aniline was added over a 35-minute period while maintaining the reaction temperature at 20℃. The reaction mixture was stirred for one hour at less than 25℃. The reaction mixture was then heated to 750C and held for two hours. Finally, the reaction mixture was heated to reflux (~90°C) and was held for five hours. The reaction mixture was cooled and the layers were separated. The top, organic layer was distilled through a 14" packed column under reduced pressure. The fraction taken at a head temperature of 140-1430C and 5 mm Hg pressure weighed 104 grams and was analyzed to contain 73% DHP for an overall yield of 46%.

3,5-Diethyl-1,2-dihydro-1-phenyl-2-propylpyridineSupplier

Jinan Liheng Biotechnology Co., Ltd. Gold
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Nanjing Norris-Pharm Technology Co., Ltd
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