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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 593902Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/593902

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 3M 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-d6) 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
PatentnummerUS09242962B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-f93c731a88cc4e44b9190ace3bfd09f6
Quellennotizuspto-grants-2016_01