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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 6-Butoxy-7-methoxy-1-(3-methoxy-benzyl)-isoquinoline-4-carbaldehyde | HCID 22048294 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Butoxy-7-methoxy-1-(3-methoxy-benzoyl)-isoquinoline-4-carbaldehyde | HCID 22048291 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067529B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-1faf942937da41df9e9d3e77f86e0cb8 |
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| Source note | uspto-grants-2006_06 |
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