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ChemicalBook CAS DataBase List 5-METHOXY-1-METHYLINDOLE-3-CARBOXALDEHYDE
39974-94-2

5-METHOXY-1-METHYLINDOLE-3-CARBOXALDEHYDE synthesis

11synthesis methods
5-Methoxyindole-3-carboxaldehyde

10601-19-1

Iodomethane

74-88-4

5-METHOXY-1-METHYLINDOLE-3-CARBOXALDEHYDE

39974-94-2

1. 5-methoxyindole-3-carboxaldehyde (300 mg, 1.71 mmol) was added to a stirring solution of sodium hydride suspension (82 mg, 2.05 mmol, 60% dispersed in mineral oil) in DMF (8 mL) in batches under argon protection, a process which needed to be completed within 5 minutes. 2. The reaction mixture was continued to be stirred for 30 minutes, followed by the addition of iodomethane (0.13 mL, 2.05 mmol) and continued stirring for 1 hour. 3. Upon completion of the reaction, 10% sodium bicarbonate solution (40 mL) was added and the mixture was extracted with ethyl acetate (4×). 4. The organic layers were combined, washed sequentially with 10% sodium bicarbonate solution (2×) and saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated. 5. The crude product was purified by column chromatography (eluent: 50:50 ethyl acetate/hexane) to afford 5-methoxy-1-methylindole-3-carbaldehyde (320 mg, 99%) as a light yellow solid. Rf = 0.35 (50:50 ethyl acetate/hexane); melting point = 130-132°C (literature value: 132-133°C). 1H NMR (CDCl3): δ 9.95 (s, 1H), 7.79 (d, 1H, J = 2.4 Hz), 7.62 (s, 1H), 7.25 (d, 1H, J = 8.8 Hz), 6.96 (dd, 1H, J = 2.4 and 8.9 Hz), 3.90 (s, 3H), 3.85 (s, 3H).

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Yield:39974-94-2 100%

Reaction Conditions:

with sodium hydride in dimethyl sulfoxide at 20; for 0.5 h;

References:

Chakrabarty, Manas;Basak, Ramkrishna;Harigaya, Yoshihiro;Takayanagi, Hiroaki [Tetrahedron,2005,vol. 61,# 7,p. 1793 - 1801]

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