HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Acetyl-5-carbomethoxy-7-chloro-4-methoxy-1,2-dihydroindole → 1-Acetyl-5-carboxy-7-chloro-4-methoxy-1,2-dihydroindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Acetyl-5-carbomethoxy-7-chloro-4-methoxy-1,2-dihydroindole | HCID 10564950 | — |
| Solvent | Sodium hydroxide methanol | HCID 23721981 | — |
| Product | 1-Acetyl-5-carboxy-7-chloro-4-methoxy-1,2-dihydroindole | HCID 14883226 | — |
Reaction Steps
A mixture of the indole ester of step 9 above (0.8 g) and 10% aqueous NaOH/MeOH (20 ml/80 ml) is stirred under reflux for 2 hours. The reaction mixture is concentrated and the aqueous residue is diluted with water and extracted with CHCl3. The organic layer is dried (MgSO4) and evaporated affording an off-white solid which is determined to be the desired compound by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04920219 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-2d6adf4bd802410b97733c9b3797b538 |
| Source note | uspto-grants-1990_04 |