HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908661Generated: November 2, 2026
Selenium Dioxide → 5-Methoxy-4-nitro-2-benzothiazolecarboxaldehyde
https://huagongshe.com/reaction/908661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | HCID 45077105 | HCID 45077105 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Methoxy-4-nitro-2-benzothiazolecarboxaldehyde | HCID 24178723 | — |
Reaction Steps
12.8 g (0.115 mol; 6 equivalents) of selenium dioxide is added to 4.34 g (19.3 mmol) of 5-methoxy-2-methyl-4-nitro-1,3-benzothiazole in solution in 180 ml of anhydrous dioxan. The reaction mixture is stirred at 80° C. for 18 hours then the insoluble part is filtered and the solvent is evaporated off under reduced pressure. The expected aldehyde is obtained in the form of a yellow oil and purified on a silica column (eluent: ethyl acetate/heptane: gradient of 30% to 70%). Melting point: 154-155° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017637B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-f82eb7ad32084fe0b74eefec86eec845 |
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| Source note | uspto-grants-2011_09 |
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