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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833151Generated: October 30, 2026

Selenium Dioxide → 6-Butoxy-7-methoxy-1-(3-methoxy-benzoyl)-isoquinoline-4-carbaldehyde

https://huagongshe.com/reaction/1833151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelenium DioxideHCID 24007—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant6-Butoxy-7-methoxy-1-(3-methoxy-benzyl)-isoquinoline-4-carbaldehydeHCID 22048294—
SolventAcetic AcidHCID 176—
Product6-Butoxy-7-methoxy-1-(3-methoxy-benzoyl)-isoquinoline-4-carbaldehydeHCID 2204829163%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a stirred solution of 6-butoxy-7-methoxy-1-(3-methoxy-benzyl)-isoquinoline-4-carbaldehyde (200 mg, 0.53 mmol) in acetic acid (5 mL) was added selenium dioxide (175 mg, 1.58 mmol). The reaction mixture was heated at 120° C. for 1 h. The solvent was evaporated and the residue was diluted with dichloromethane (30 mL). The organic layer was washed with saturated aqueous sodium bicarbonate solution (20 mL), saturated aqueous sodium chloride solution (20 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to afford a crude oil. Flash chromatography (Merck Silica gel 60, 70–230 mesh, 40% ethyl acetate/hexane) afforded 6-butoxy-7-methoxy-1-(3-methoxy-benzoyl)-isoquinoline-4-carbaldehyde as a yellow solid (131 mg, 63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067529B2
Source datasetuspto-grants-2006_06
ORD IDord-1faf942937da41df9e9d3e77f86e0cb8
Source noteuspto-grants-2006_06