HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20270201, compound → HCID 20270193, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20270201 | HCID 20270201 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 20270193 | HCID 20270193 | — |
Reaction Steps
A solution of crude 3-[(p-ethoxycarbonylphenoxy)methyl]-N-(3-pyridyl)-indole (6.5 g) in 60 ml of ethanol and 60 ml of 1N sodium hydroxide is heated under reflux for 3 hours. The ethanol is distilled off, the aqueous phase is washed with ether, acidified with conc. hydrochloric acid to pH=6, and the resulting solid is filtered off to yield 3-[(p-carboxyphenoxy)-methyl]-N-(3-pyridyl)indole. Treatment with ethanolic hydrogen chloride gives 3-[(p-carboxyphenoxy)methyl]-N-(3-pyridyl)indole hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536505 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-380751b63ba0458eaef47a49bf482ed6 |
| Source note | uspto-grants-1985_08 |