HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 5-Methoxy-4,6,7-trimethylindole-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 5-methoxy-4,5,7-trimethylindole-2-carboxylate | HCID 19418845 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Methoxy-4,6,7-trimethylindole-2-carboxylic acid | HCID 19418789 | — |
Reaction Steps
A solution of ethyl 5-methoxy-4,5,7 trimethylindole-2-carboxylate (PREPARATION 19, 1.04 g) in ethanol (30 ml) containing potassium hydroxide (45%, 2.5 ml) is heated under reflux for 1.5 hr. The mixture is acidified with acetic acid (2 ml) and concentrated under reduced pressure. The residue is mixed with water (200 ml) and filtered. The filter cake is washed with water and dried to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05489593 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-028c4db8e8614fac8891008e711f015f |
| Source note | uspto-grants-1996_02 |