HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 5-methoxyindole-2-carboxylate → Ethyl 4-bromo-5-methoxy-1H-indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 5-methoxyindole-2-carboxylate | HCID 20926 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 4-bromo-5-methoxy-1H-indole-2-carboxylate | HCID 11460715 | 100% |
Reaction Steps
To a suspension of ethyl 5-methoxy-1H-indole-2-carboxylate (5 g, 22.81 mmol) in acetic acid (100 mL) was added bromine (1.169 mL, 22.81 mmol) slowly at room temperature. The reaction mixture was stirred at room temperature for 2 days. The solid was filtered off, washed with acetic acid and hexanes, and dried to give the title compound as a white solid (6.8 g). LCMS m/z=298.6 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108969B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-44b0e97028664c8189804bdb98e3a482 |
| Source note | uspto-grants-2015_08 |