HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404191Generated: October 31, 2026
Water → 5-(4-tert-Butyl-cyclohexyloxy)-benzothiazole-2-carbaldehyde
https://huagongshe.com/reaction/2404191
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 5-(4-tert-Butyl-cyclohexyloxy)-2-methyl-benzothiazole | HCID 66926585 | — |
| Product | 5-(4-tert-Butyl-cyclohexyloxy)-benzothiazole-2-carbaldehyde | HCID 86668428 | — |
Reaction Steps
Selenium dioxide (180 mg, 1.6 mmol) was combined with 1,4-Dioxane (5 mL, 60 mmol) and Water (0.5 mL, 30 mmol) at room, temperature open to the atmosphere. The mixture was then treated with 5-(4-tert-Butyl-cyclohexyloxy)-2-methyl-benzothiazole (250 mg, 0.82 mmol) and resulting mixture was heated to 65° C. for 2 hours. The heat was increased to 90° C. and 4 additional eq. of SeO2 were added. Reaction was stirred for additional 5 hours. LCMS shows nearly complete conversion. Reaction become dark and solids formed in reaction mixture. Reaction was cooled to RT and allowed to stand over night. Solids were removed via filtration. Concentrated to dryness then purified directly via column chromatography using a gradient of 0-40% Ethylacetate/hexane to give the title compound as a dark solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802659B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-4f5ba1f39cc74608b9cdf6d708397e3b |
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| Source note | uspto-grants-2014_08 |
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