HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 20041368, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 5-Cyanotryptamine | HCID 58926 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20041368 | HCID 20041368 | 51.1% |
Reaction Steps
Freshly distilled benzaldehyde (2.96 g) was added to a solution of 3-(2-aminoethyl)-1H-indole-5-carbonitrile (5 g) in absolute ethanol (120 ml). The mixture was heated at reflux for 2 h before cooling to 10°. Sodium borohydride (1 g) was added and the suspension stirred for 2 h. The mixture was reduced to dryness and the residue recrystallised from a mixture of toluene and petroleum ether (b.p. 60°-80°). The solid was washed well with water and dried to give the title compound as a powder (3.8 g), m.p 99°-101°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04833153 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-4421b81fe0ac46beb4d752b49596856b |
| Source note | uspto-grants-1989_05 |