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ChemicalBook CAS DataBase List 6-Chloro-5-methylindoline

6-Chloro-5-methylindoline synthesis

4synthesis methods
162100-42-7 Synthesis
6-Chloro-5-Methyl 1H-indole

162100-42-7
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$60.00/2mg

6-Chloro-5-methylindoline

162100-44-9
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Yield:162100-44-9 3.5 g

Reaction Conditions:

with sodium cyanoborohydride;acetic acid at 20; for 1 h;Inert atmosphere;Industrial scale;

Steps:

1.4 Step 4:

To a solution of Compound D (3.5 g, 21 mmol) in AcOH (40 mL) was added sodium cyanoborohydride (2.7 g, 43 mmol) and the mixture was purged with N2 for 1 h at room temperature.The reaction was complete by TLC (PE / EA = 10/1), further ethyl acetate EA (200 ml) was added and the mixture was made basic with a 5N NaOH solution (200 ml) at a pH of about 8. The organic layer was separated, Wash once, fullAnd brine once, dried over anhydrous sodium sulfate, dried to give 3.5g of brown solid Compound E, spare. Yield 98%.

References:

CN106278987,2017,A Location in patent:Paragraph 0033; 0038

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