HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methyl cyanoacetate → Indole
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methyl cyanoacetate | HCID 7747 | — |
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | 1H-Indole-3-carboxaldehyde, 1-methyl-2-phenyl- | HCID 74468 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Indole | HCID 798 | 263,8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08361625B2 |
| Quelldatensatz | uspto-grants-2013_01 |
| ORD ID | ord-49669eb5cbd143bb9afba59f582bd187 |
| Quellennotiz | uspto-grants-2013_01 |