HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 7-(benzyloxy)-4-formyl-1H-indole-2-carboxylate → 7-(Benzyloxy)-4-formyl-1H-indole-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 7-(benzyloxy)-4-formyl-1H-indole-2-carboxylate | HCID 13243484 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 7-(Benzyloxy)-4-formyl-1H-indole-2-carboxylic acid | HCID 13243485 | 107.6% |
Reaction Steps
2.26 g of 7-benzyloxy-4-formylindole-2-carboxylic acid ethyl ester is heated in a mixture of 15 ml of 1N sodium hydroxide solution and 15 ml of ethanol for one hour to 100° C. The ethanol is then distilled off under vacuum, the mixture is acidified with 10% hydrochloric acid and the precipitate is vacuum-filtered. The product is recrystallized from glacial acetic acid, thus obtaining 2.22 g of 7-benzyloxy-4-formylindole-2-carboxylic acid, mp 207° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04835175 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-cef7baf402e546d8b689c04c55db1920 |
| Source note | uspto-grants-1989_05 |