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Chemical Structure| 81039-18-1 Chemical Structure| 81039-18-1

Structure of 81039-18-1

Chemical Structure| 81039-18-1

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Product Details of [ 81039-18-1 ]

CAS No. :81039-18-1
Formula : C9H10N2
M.W : 146.19
SMILES Code : CC(C1=NC=CC=C1)(C)C#N
MDL No. :MFCD09753941

Safety of [ 81039-18-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 81039-18-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 81039-18-1 ]

[ 81039-18-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 81039-18-1 ]
  • [ 199296-39-4 ]
YieldReaction ConditionsOperation in experiment
With lithium aluminium tetrahydride; In diethyl ether; Step B 2-Methyl-2-(2-pyridyl)-1-propylamine To a solution of 2-methyl-2-(2-pyridyl)-propionitrile (1.018 g, 6.97 mmol) in 25 mL of anhydrous diethyl ether under a blanket of Argon was added LiAlH4 (0.538 g, 14.17 mmol) portionwise. After 1 h the reaction was quenched with the addition of water (1 mL), NaOH (1.0 mL, 1N), water (8 mL) then diethyl ether (20 mL) and let stir for 10 h. The solution was filtered through a plug of celite and washed with diethyl ether:MeOH (1:1) (200 mL). The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography (30*150 mm column of SiO2, CH2 Cl2 /CH2 Cl2 saturated with NH3 /MeOH gradient elution 60:39:1 to 60:38:2 to 60:37:3) to give the title compound as a resin: 1 H NMR (400 MHz, CDCl3) d 1.21 (br s, 2H), 1.38 (s, 6H), 2.98 (s, 2H), 7.05-7.14 (m, 1H), 7.34-7.38 (m, 1H), 7.60-7.64 (m, 1H), 8.59-8.61 (m, 1H).
With lithium aluminium tetrahydride; In diethyl ether; Step B: 2-Methyl-2-(2-pyridyl)-1-propylamine To a solution of 2-methyl-2-(2-pyridyl)-propionitrile (1.018 g, 6.97 mmol) in 25 mL of anhydrous diethyl ether under a blanket of Argon was added LiAlH4 (0.538 g, 14.17 mmol) portionwise. After 1 h the reaction was quenched with the addition of water (1 mL), NaOH (1.0 mL, 1N), water (8 mL) then diethyl ether (20 mL) and let stir for 10 h. The solution was filtered through a plug of celite and washed with diethyl ether:MeOH (1:1) (200 mL). The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography (30 x 150 mm column of SiO2, CH2Cl2/CH2Cl2 saturated with NH3/MeOH gradient elution 60:39:1 to 60:38:2 to 60:37:3) to give the title compound as a resin: 1H NMR (400 MHz, CDCl3) d 1.21 (br s, 2H), 1.38 (s, 6H), 2.98 (s, 2H), 7.05-7.14 (m, 1H), 7.34-7.38 (m, 1H), 7.60-7.64 (m, 1H), 8.59-8.61 (m, 1H).
 

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