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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713970Generated: November 1, 2026

Water → 5-(4-tert-Butyl-cyclohexyloxy)-benzothiazole-2-carbaldehyde

https://huagongshe.com/reaction/713970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSelenium DioxideHCID 24007—
Reactant1,4-DioxaneHCID 31275—
Reactant5-(4-tert-Butyl-cyclohexyloxy)-2-methyl-benzothiazoleHCID 66926585—
Product5-(4-tert-Butyl-cyclohexyloxy)-benzothiazole-2-carbaldehydeHCID 86668428—

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186367B2
Source datasetuspto-grants-2015_11
ORD IDord-91e75605b8da4e308f0bbc8653d62acd
Source noteuspto-grants-2015_11