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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 516781Erstellt: 25. Oktober 2026

Methanol → 6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylic acid

https://huagongshe.com/reaction/516781

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktSodium HydroxideHCID 14798—
Eduktmethyl 6-cyano-1-isopropyl-3-methyl-1H-indole-4-carboxylateHCID 67467281—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylic acidHCID 6746808964,2%

Reaktionsschritte

To a 50 ml round bottom was added methyl 6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylate (230 mg, 0.897 mmol), followed by methanol (1 mL) and THF (1 mL). To the solution was added 3 M NaOH (0.449 mL, 2.69 mmol). The reaction stirred at rt for 20 h. The reaction was evaporated and treated with acidic water to pH 5. A brown solid crashed out and was collected by filtration. The solid was an impurity. The pH of the liquid was adjusted to 3 and the liquid was evaporated leaving a residue. Trituration of the residue with water, followed by filtration yielded 6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylic acid (155 mg, 0.576 mmol, 64.2% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-β6) δ ppm 13.16 (br. s., 1H) 8.33 (s, 1H) 7.78 (s, 1H) 7.66 (s, 1H) 4.81-4.98 (m, 1H) 2.33 (s, 4H) 1.45 (d, J=6.57 Hz, 6H). MS(ES) [M+H]+ 243.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09114141B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-7aa0dc5276e94aa6b6f2b3833f1b6a19
Quellennotizuspto-grants-2015_08