HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405696Generated: October 26, 2026
Cuminol → 3-{[4-(1-Methylethyl)benzyl]oxy}pyridin-2-amine
https://huagongshe.com/reaction/1405696
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cuminol | HCID 325 | — |
| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Amino-3-bromopyridine | HCID 817700 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 3-{[4-(1-Methylethyl)benzyl]oxy}pyridin-2-amine | HCID 28981792 | 65.7% |
Reaction Steps
A mixture of cesium carbonate (2.82 g), 1,10-phenanthrolin (0.208 g), (4-isopropylphenyl)methanol (8.68 g), 3-bromopyridin-2-amine (1 g) and copper (I) iodide (0.110 g) in toluene (10 mL) was stirred under a nitrogen atmosphere at 110° C. overnight, and at 130° C. for 5 hr. The reaction mixture was added to saturated brine, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (0.92 g) as a pale-yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916551B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-cf3476a2b0734bb5a6812b2c7b8db6de |
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| Source note | uspto-grants-2014_12 |
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