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CAS No. : | 98600-34-1 | MDL No. : | MFCD05864695 |
Formula : | C9H6BrNO | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | IPAFHZDRYAWZOB-UHFFFAOYSA-N |
M.W : | 224.05 | Pubchem ID : | 2763178 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
49% | Stage #1: With sodium tetrahydroborate In methanol; formamide at 20℃; for 0.25 h; Stage #2: at 55℃; for 16 h; |
General procedure: To a flask containing a 3-formyl-indole derivative (1.0 equiv) and sodium borohydride (3.0 equiv), methanol (9mL for 1.0mmol of starting material) and formamide (9mL for 1.0mmol of starting material) were added and stirred at room temperature for 15min. The mixture was added to potassium cyanide (10.0 equiv) prepared in a separate flask and stirred at 55°C for 16h. The reaction was quenched by adding brine and a few drops of 5N NaOH, followed by extraction with dichloromethane thrice. The combined organic layer was washed with brine, dried over anhydrous sodium sulphate and concentrated in vacuo. Purification by flash silica gel column chromatography afforded the indole-3-acetonitrile derivative product. |
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