HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 4,6-dimethoxy-2,3-dihydro-1H-indole-2,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Benzenamine, 3,5-dimethoxy-, hydrochloride (1:1) | HCID 218603 | — |
| Product | 4,6-dimethoxy-2,3-dihydro-1H-indole-2,3-dione | HCID 11557522 | 100% |
Reaction Steps
12 g (63 mmol) of 3,5-dimethoxyaniline hydrochloride and 20 ml (230 mol) of oxalyl chloride were stirred at 165° C. for 30 min. The excess of oxalyl chloride was distilled (the color of the reaction mixture changed from dark-red to green-yellow). The reaction mixture was cooled and methanol was added. The resulting suspension was heated then filtered, washed with methanol and dried to yield 13 g of 4,6-dimethoxyindole-2,3-dione (100% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07381730B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-37dc510889a84c359231f537edcf0396 |
| Source note | uspto-grants-2008_06 |