HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334830Generated: October 26, 2026
3,3,5-Trimethylcyclohexanol → HCID 67294303, compound
https://huagongshe.com/reaction/334830
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,3,5-Trimethylcyclohexanol | HCID 8298 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenol | HCID 54751948 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67294303 | HCID 67294303 | 72.7% |
Reaction Steps
2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenol (0.8 g, 2.9 mmol) is partly solved in dioxane (23 mL) at 80° C. 3,3,5-Trimethyl-cyclohexanol (12.3 g, 86 mmol) and sodium hydride (200 mg, 5 mmol, 60% in mineral oil) are added subsequently. The orange reaction mixture is stirred at 70° C. for one hour and evaporated to dryness. The residue is dissolved in ethyl acetate and extracted with water. The organic layer is dried over sodium sulphate, filtered and evaporated to dryness. The crude product is purified by column chromatography (ethyl acetate/heptane 1:4) to yield 0.8 g of 2-(2H-Benzotriazol-2-yl)-6-(3,3,5-trimethyl-cyclohexyloxymethyl)-4-methyl-phenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883829B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-e6c43fb0191240869cb25eb55521a5ba |
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| Source note | uspto-grants-2014_11 |
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