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ChemicalBook CAS DataBase List 4-Bromo-1H-indole-2-carbonitrile
955978-74-2

4-Bromo-1H-indole-2-carbonitrile synthesis

2synthesis methods
4-Bromo-1H-indole-2-carboxamide

955978-73-1
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4-Bromo-1H-indole-2-carbonitrile

955978-74-2
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Yield: 82%

Reaction Conditions:

with trichlorophosphate in toluene for 0.75 h;Heating / reflux;

Steps:

13
Phosphorous oxychloride (1.9 mL, 20 mmol) was added to a suspension of 4-bromo- lH-indole-2-carboxylic acid amide (1.32 g, 5.5 mmol.) in toluene (10 mL) and the mixture was stirred at reflux for 45 min. On cooling, the mixture was poured into an aqueous Na2CO3 solution (sat., 50 mL) and the mixture stirred until effervescence had subsided. The layers were separated, the aqueous phase extracted with EtOAc and the combined organic layers dried (MgSO4) and evaporated to dryness. The crude material was purified by column chromatography to afford the title compound as a solid (1.00 g, 82 %). NMR δη (400 MHz, CDCl3) 7.22-7.28 (m, 2H), 7.35-7.40 (m, 2H) and 8.79 (s, IH).

References:

Location in patent:Page/Page column 55

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