ChemicalBook CAS DataBase List 5-Chloroindole-3-acetonitrile

5-Chloroindole-3-acetonitrile synthesis

6synthesis methods

Product Name:5-Chloroindole-3-acetonitrile
CAS Number:81630-83-3
Molecular formula:C10H7ClN2
Molecular Weight:190.63

87-52-5 Synthesis

87-52-5
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$16.00/5g

17422-32-1 Synthesis

17422-32-1
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$6.00/1g

74-88-4
350 suppliers
$15.00/10g

81630-83-3
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Yield:81630-83-3 63%

Reaction Conditions:

with sodium hydroxide;formaldehyd;tetrabutyl ammonium fluoride;acetic acid;dimethyl amine in tetrahydrofuran;dichloromethane;water;ethyl acetate;toluene;

Steps:

24.1 1)

1) Preparation of (5-chloro-1H-indol-3-yl)-acetonitrile To a solution of 5-chloroindole (1.0 g, 6.8 mmol, 1.0 eq.) in a mixture of acetic acid (2 mL) and water (1 mL) were added, at 0°C, formaldehyde (720 μL, 37% in H₂O, 8.9 mmol, 1.3 eq) and dimethylamine (1.23 mL, 40% in H₂O, 10.9 mmol, 1.7 eq). The mixture was stirred at room temperature for 6 hours and then, quenched with ice and 5 M aqueous sodium hydroxide. The mixture was extracted with dichloromethane and then, the organic layer was dried over MgSO₄ and partially evaporated. To the solution gramine in dichloromethane (20 mL) were added, under an argon atmosphere, anhydrous toluene (40 mL) and methyl iodide (824 μL, 13.2 mmol, 2.0 eq.). The mixture was stirred at room temperature for 12 hours and then, concentrated under reduced pressure. To the residue taken up in anhydrous THF (60 mL) were added, under an argon atmosphere, TMSCN (1.25 mL, 9.9 mmol, 1.5 eq.) and TBAF (19.9 mL, 1M, 19.9 mmol, 3.0 eq.). The mixture was stirred at room temperature for 4 hours and then, concentrated under reduced pressure. The crude was taken up in ethyl acetate and the organic layer was washed with aqueous bicarbonate solution and then dried over MgSO₄. The solvent was removed under reduced pressure, and the residue purified by silica gel pad filtration (eluent: EtOAc) to afford (5-chloro-1H-indol-3-yl)-acetonitrile as a beige solid (0.80 g, 63%).

References:

EP2266562,2010,A1

50-00-0 Synthesis