5-Bromoindole-3-acetonitrile synthesis
- Product Name:5-Bromoindole-3-acetonitrile
- CAS Number:774-14-1
- Molecular formula:C10H7BrN2
- Molecular Weight:235.08
830-93-3
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7677-24-9
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74-88-4
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774-14-1
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Yield:774-14-1 51%
Reaction Conditions:
with tetrabutyl ammonium fluoride in tetrahydrofuran;hexane;water;ethyl acetate;benzene;
Steps:
63.2 (5-Bromo-1H-indol-3-yl)-acetonitrile
Step 2 (5-Bromo-1H-indol-3-yl)-acetonitrile To an ice cooled suspension of (5-bromo-1H-indol-3-ylmethyl)-dimethyl-amine (11.2 g, 44.1 mmol) in benzene (145 mL) was added iodomethane (8.2 mL, 130 mmol). The reaction mixture was stirred overnight at room temperature and concentrated. The residue was dissolved in THF (210 mL). Trimethylsilyl cyanide (11.7 mL, 87.7 mmol) and tetrabutylammonium fluoride (140 mL, 140 mmol of a 1.0 M solution in THF) were added. After stirring for 2.5 hours, at room temperature, water (12 mL) was added. The mixture was partially concentrated. The residue was partitioned in ethyl acetate and water. The organic phase was washed with water and brine, dried over anhydrous magnesium sulfate and evaporated to dryness. Purification by flash chromatography using 15-35% ethyl acetate in hexane as an eluant afforded (5-bromo-1H-indol-3-yl)-acetonitrile (5.30 g, 51%) as a mauve solid, mp 105-106° C. 1H-NMR (300 MHz, DMSO-d6): δ11.35 (s, 1H), 7.8 (d, 1H, J=2.2 Hz), 7.35-7.45 (m, 2H), 7.2-7.3 (m, 1H), and 4.0 ppm (s, 2H).
References:
US2003/125371,2003,A1
10075-50-0
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774-14-1
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773837-37-9
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10075-50-0
694 suppliers
$5.00/10g
74-88-4
348 suppliers
$15.00/10g
774-14-1
35 suppliers
inquiry
830-93-3
65 suppliers
$60.00/500mg
774-14-1
35 suppliers
inquiry