Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 475494Erstellt: 25. Oktober 2026

Indole-3-Acetic Acid → Methyl indole-3-acetate

https://huagongshe.com/reaction/475494

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndole-3-Acetic AcidHCID 802—
EduktMethanolHCID 887—
EduktSulfuric AcidHCID 1118—
EduktSodium HydroxideHCID 14798—
LösungsmittelWaterHCID 962—
LösungsmittelPotassium CarbonateHCID 11430—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
ProduktMethyl indole-3-acetateHCID 7470681%

Reaktionsschritte

Concentrated sulfuric acid (0.2 equiv.) was carefully added to a solution of 1H-indol-3-ylacetic acid in MeOH (1 M) and the reaction was stirred at rt for 2.5 h. The solution was cooled with an ice bath, and aqueous 2 N NaOH (0.18 equiv.) was slowly added such that T<10° C. The solution was diluted with water, and solid K2CO3 was then added until pH was neutral. The solution was extracted with MTBE (2×), washed with water (2×), brine, dried over Na2SO4, filtered, and concentrated to give a brown syrup. The crude syrup was dissolved in MTBE (1.4 mL/g) and transferred to a three necked flask fitted with a temperature probe, mechanical stirrer, addition funnel and nitrogen inlet. Hex was then slowly added to the stirring solution over 1 h. More Hex was then added over 2 h then left overnight. The suspension was filtered, washed with Hex, and dried on the fit under nitrogen for 20 h to give the title compound (81%) as a light orange solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08637541B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-41c26aec9edf4605ba206389eaaf79aa
Quellennotizuspto-grants-2014_01