HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833141Generated: October 31, 2026
Selenium Dioxide → 6-Benzyloxy-7-methoxy-1-(3-methoxy-benzoyl)-isoquinoline-4-carbaldehyde
https://huagongshe.com/reaction/1833141
Participants
| Role | Name | HCID | Charge |
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| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 6-Benzyloxy-7-methoxy-1-(3-methoxy-benzyl)-isoquinoline-4-carbaldehyde | HCID 22048347 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Benzyloxy-7-methoxy-1-(3-methoxy-benzoyl)-isoquinoline-4-carbaldehyde | HCID 22048395 | 57% |
Reaction Steps
To a stirred solution of 6-benzyloxy-7-methoxy-1-(3-methoxy-benzyl)-isoquinoline-4-carbaldehyde (90 mg, 0.22 mmol) in acetic acid (3 mL) was added selenium dioxide (120 mg, 1.08 mmol). The reaction mixture was heated at 120° C. for 1 hr. 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-benzyloxy-7-methoxy-1-(3-methoxy-benzoyl)-isoquinoline-4-carbaldehyde as a yellow solid (50 mg, 57% 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-d87597efe87f44c7955075fc227dc5a4 |
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| Source note | uspto-grants-2006_06 |
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