HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-ethyl-6-fluoro-3-(hydroxymethyl)-7,8-bis((4-methoxybenzyl)oxy)quinolin-4(1H)-one → 1-Ethyl-6-fluoro-7,8-bis((4-methoxybenzyl)oxy)-4-oxo-1,4-dihydroquinoline-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-ethyl-6-fluoro-3-(hydroxymethyl)-7,8-bis((4-methoxybenzyl)oxy)quinolin-4(1H)-one | HCID 86732812 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Ethyl-6-fluoro-7,8-bis((4-methoxybenzyl)oxy)-4-oxo-1,4-dihydroquinoline-3-carbaldehyde | HCID 86732813 | 76.1% |
Reaction Steps
To a yellow solution of 1-ethyl-6-fluoro-3-(hydroxymethyl)-7,8-bis((4-methoxybenzyl)oxy) quinolin-4(1H)-one (33 g, 66.9 mmol) in Dichloromethane (DCM) (200 mL) was added manganese dioxide (58.1 g, 669 mmol), and the mixture was stirred at rt for 6.5 h. The mixture was then filtered through Celite and the solid was washed with DCM. The filtrate was concentrated in vacuo to afford 1-ethyl-6-fluoro-7,8-bis((4-methoxybenzyl)oxy)-4-oxo-1,4-dihydroquinoline-3-carbaldehyde (25 g, 50.9 mmol, 76% yield) as a yellow solid, which was used in the next step without further purification. LCMS: (M+H)+: 492.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340556B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-2664826780214cbf9b1470a39a0b3c70 |
| Source note | uspto-grants-2016_05 |