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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525944Generated: October 28, 2026

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

https://huagongshe.com/reaction/525944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ethyl-6-fluoro-3-(hydroxymethyl)-7,8-bis((4-methoxybenzyl)oxy)quinolin-4(1H)-oneHCID 86732812—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product1-Ethyl-6-fluoro-7,8-bis((4-methoxybenzyl)oxy)-4-oxo-1,4-dihydroquinoline-3-carbaldehydeHCID 8673281376.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340556B2
Source datasetuspto-grants-2016_05
ORD IDord-2664826780214cbf9b1470a39a0b3c70
Source noteuspto-grants-2016_05