HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → Ketone, indol-3-yl p-methoxyphenyl (6CI,8CI)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ketone, indol-3-yl p-methoxyphenyl (6CI,8CI) | HCID 211017 | — |
Reaction Steps
30 ml of ether solution containing 4.0 g of indole were added to 10 ml of ether solution containing 5.0 g of methylmagnesium iodide. And then 30 ml of ether solution containing 5.7 g of anisoyl chloride were added dropwise to the solution. The reaction mixture was allowed to stand for several hours and further refluxed for 3 hours. After cooling, the reaction mixture was washed with aqueous solution of sodium hydrogencarbonate. The obtained organic layer was evaporated to dryness under reduced pressure. After purification by chromatography on silica gel and recrystallization from ethanol, 3-(p-methoxybenzoyl)indole (compound 1) was obtained in the form of white crystals. (Yield: 42%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04708961 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-654df088391c4892a801d584e25a06a9 |
| Source note | uspto-grants-1987_11 |