HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637762Generated: November 1, 2026
Selenium Dioxide → 5,6,7,8-Tetrahydroisoquinoline-1-carbaldehyde
https://huagongshe.com/reaction/1637762
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | HCID 18799883 | HCID 18799883 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5,6,7,8-Tetrahydroisoquinoline-1-carbaldehyde | HCID 18799671 | 90.1% |
Reaction Steps
1-Hydroxymethyl-5,6,7,8-tetrahydroisoquinoline (4.14 g, 25.4 mmole) is dissolved in 75 ml dioxane in a 200 ml one neck round bottom flask under nitrogen. The solution is treated with selenium dioxide (1.56 g, 14.0 mmole) and the reaction mixture is warmed to 80-85° C. for 2.5 h. The mixture is cooled to room temperature, is diluted with 125 ml dichloromethane and is filtered through celite. The filter cake is washed well with fresh dichloromethane and the filtrate is concentrated in vacuo to an amber oil. The crude material is chromatographed over 200 g silica gel (230-400 mesh), eluting with 1:5:4 acetone/chloroform/hexane while collecting 50 ml fractions. Fractions 11-18 are combined and concentrated to give 3.69 g (90%) of 5,6,7,8,-tetrahydroisoquinoline-1-carbaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06043248 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-22fd1138cc7f449cae394525eaf34478 |
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| Source note | uspto-grants-2000_03 |
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