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 | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N,N-dimethyl-p-methoxybenzamide | HCID 81713 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ketone, indol-3-yl p-methoxyphenyl (6CI,8CI) | HCID 211017 | 56% |
Reaction Steps
2.6 g of indole and 8.6 g of N,N-dimethylanisamide were added to 2.6 ml of phosphorus oxychloride. The mixture was heated at 80°-85° C. for 3 hours. After cooling,50 ml of ether was added to the mixture. The reaction mixture was then poured into water and pH value was adjusted to 10 with aqueous solution of sodium hydroxide. The resulting precipitate was filtered out and then recrystallized from ethanol to obtain compound 1 in the form of white crystals. (Yield: 56%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04708961 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-6025311c4c8c4182b0f8ff44a0e8297d |
| Source note | uspto-grants-1987_11 |