HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029042Generated: November 1, 2026
1,10-Phenanthroline → 2-Bromo-1-methyl-3-(neopentyloxy)benzene
https://huagongshe.com/reaction/1029042
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Neopentyl alcohol | HCID 6404 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Bromo-1-iodo-3-methylbenzene | HCID 50998158 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Bromo-1-methyl-3-(neopentyloxy)benzene | HCID 67325713 | — |
Reaction Steps
A vial was charged with 2-bromo-1-iodo-3-methylbenzene (677 mg, 2.28 mmol), neopentyl alcohol (2.21 g, 25.08 mmol), copper(I) iodide (43.4 mg, 0.228 mmol), 1,10-phenanthroline (82 mg, 0.456 mmol) and cesium carbonate (1.04 mg, 3.19 mmol). The vial was sealed under air atmosphere and heated to 110° C. for 24 h. The reaction mixture was cooled to rt and diethyl ether was added. The suspension was filtered through a pad of silica gel. The solvent was removed under reduced pressure and the remaining residue was purified by flash chromatography (100% hexanes). 2-Bromo-1-methyl-3-(neopentyloxy)benzene was obtained 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-9b910a8d104a44dda92de3b12f1c731f |
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| Source note | uspto-grants-2014_05 |
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