HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029041Generated: November 2, 2026
1,10-Phenanthroline → HCID 58452045, compound
https://huagongshe.com/reaction/1029041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Neopentyl alcohol | HCID 6404 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Bromo-2-iodobenzene | HCID 11415 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Product | HCID 58452045 | HCID 58452045 | — |
Reaction Steps
A vial was charged with 1-bromo-2-iodobenzene (627 μL, 5 mmol), neopentyl alcohol (4.85 g, 55.0 mmol), copper(I) iodide (95 mg, 0.500 mmol), 1,10-phenanthroline (180 mg, 1.000 mmol) and cesium carbonate (2.28 g, 7.00 mmol). The vial was sealed under air atmosphere and heated to 100° C. for 12 h. The reaction mixture was cooled to RT and filtered through a pad of silica gel. The silica gel was washed with Et2O. The filtrate was concentrated and the residue was purified by column chromatography (100% hexanes) to yield the 1-bromo-2-(neopentyloxy)benzene as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735384B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-9c70765000ba48edb697a7623c3d6e48 |
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| Source note | uspto-grants-2014_05 |
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