HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 314717, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-[(4-Chlorophenoxy)methyl]-1-methyl-1H-indole | HCID 21195985 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 314717 | HCID 314717 | — |
Reaction Steps
Under a nitrogen atmosphere 4-methylpiperidine (0.109 ml, 0.09 g, 0.92 mmol), dissolved in 2.0 ml of ethyl acetate, was added to a round bottom flask which was then placed in an ice bath. Concentrated hydrochloric acid (0.084 ml) was then added and the reaction mixture was removed from the ice bath. To the reaction mixture were added formaldehyde (0.304 g, 1.01 mmol), sodium acetate (0.113 g, 1.38 mmol), and 1-methyl-2-(4-chlorophenoxymethyl)-1H-indole (0.250 g, 0.92 mmol). The resulting mixture was then heated to reflux and maintained at this temperature overnight. The progress of the reaction was monitored by thin layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06245761B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-c54c517730a2470e9ea808fc56c5b5cc |
| Source note | uspto-grants-2001_06 |