HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-(p-Hydroxy)benzoyl indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ketone, indol-3-yl p-methoxyphenyl (6CI,8CI) | HCID 211017 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Product | 3-(p-Hydroxy)benzoyl indole | HCID 3062671 | — |
Reaction Steps
1 g of compound 1 and 3 g of pyridine hydrochloride were heated at 215° C. for 1 hour in a nitrogen atmosphere. After the mixture was cool,1.5 N hydrochloric acid was added thereto and then the supernatant was removed by centrifugation. The precipitate was dissolved in methanol which contains 10% of aqueous solution of sodium hydroxide, followed by filtering out the resulting precipitate. The obtained solution was acidified to give a crude product. The crude product was recrystallized from ethyl acetate to give 3-(p-hydroxybenzoyl)indole (compound 3). (Yield: 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04708961 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-f469414041a84f208baac4b6b4640a13 |
| Source note | uspto-grants-1987_11 |