HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(3',5'-Dimethoxy-4'-hydroxy-phenyl)-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(3',5'-Dimethoxy-4'-benzenesulphonyloxy-phenyl)-indole | HCID 22756126 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(3',5'-Dimethoxy-4'-hydroxy-phenyl)-indole | HCID 22752016 | 80% |
Reaction Steps
Into a reactor were introduced 10 ml of water containing 4.8g of solid sodium hydroxide, 30 ml of methanol and 75.6g (0.02 mol) of 2-(3',5'-dimethoxy-4'-benzenesulphonyloxy-phenyl)-indole. The reaction medium was heated to 50°-55° C., was stirred for 1 hour and was poured into an aqueous solution of hydrochloric acid. The indole derivative was extracted with ether and the ethereal phase was washed with water to neutrality, dried, treated with charcoal and, finally concentrated under reduced pressure to give 2-(3',5'-dimethoxy-4'-hydroxy-phenyl)-indole which was recrystallized from a mixture of ethanol-acetone 60/40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04129572 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-1804f64c69a447309bc69c42b5af627f |
| Source note | uspto-grants-1978_12 |