HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12628585, compound → Ethyl 3-methyl-1H-indole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12628585 | HCID 12628585 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 3-methyl-1H-indole-5-carboxylate | HCID 12628587 | 73.1% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a solution of 2-bromo-4-carboethoxy-N-allylaniline (J. Org. Chem., 45, 2710 (1980)) (650 mg, 2.29 mmol) in acetonitrile (10 ml), tetrakis(triphenylphosphine)palladium(0) (132 mg, 0.114 mmol), palladium (II) acetate (25.7 mg, 0.114 mmol) and TEA (0.413 ml, 2.98 mmol) were added and stirred overnight in a sealed tube at 100° C. After filtering the reaction mixture, the filtrate was evaporated under reduced pressure; the thus obtained residue was subjected to silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:2) to give the titled compound (340 mg, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06586630B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-222068574c3146c29a34528ae0c00e15 |
| Source note | uspto-grants-2003_07 |