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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1808672Erstellt: 25. Oktober 2026

Methyl cyanoacetate → Indole

https://huagongshe.com/reaction/1808672

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl cyanoacetateHCID 7747—
EduktPiperidineHCID 8082—
Edukt1H-Indole-3-carboxaldehyde, 1-methyl-2-phenyl-HCID 74468—
LösungsmittelMethanolHCID 887—
ProduktIndoleHCID 798263,8%

Reaktionsschritte

To 120 ml of methanol were added 23.5 g (0.10 mol) of 1-methyl-2-phenyl-1H-indole-3-carbaldehyde and 11.9 g (0.12 mol) of methyl cyanoacetate to produce a mixture. Subsequently, 2.5 g (0.03 mol) of piperidine was added to the mixture, reacted under reflux for 6 hours, and cooled to room temperature to precipitate a crystal. The obtained crystal was washed with a small amount of methanol, and then dried to give 30.9 g of a light-yellow crystalline indole compound A having a structure of the general Chemical Formula (1) in which R1 was methyl group and R2 was methyl group. The melting point of the obtained indole compound A was 193.7° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08361625B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-49669eb5cbd143bb9afba59f582bd187
Quellennotizuspto-grants-2013_01