HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179255Generated: October 30, 2026
1,10-Phenanthroline → 1-methoxy-4-[(2-methylprop-2-en-1-yl)oxy]benzene
https://huagongshe.com/reaction/2179255
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Methallyl alcohol | HCID 10557 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Iodoanisole | HCID 69676 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-methoxy-4-[(2-methylprop-2-en-1-yl)oxy]benzene | HCID 257962 | 78% |
Reaction Steps
A test tube was charged with CuI (20 mg, 0.10 mmol, 0.10 equiv), 1,10-phenanthroline (36 mg, 0.20 mmol, 0.20 equiv), Cs2CO3 (652 mg, 2.0 mmol, 2.0 equiv), 4-iodoanisole (234 mg, 1.0 mmol, 1.0 equiv), 2-methyl-2-propen-1-ol (168 μL, 2.0 mmol, 2.0 equiv) and toluene (0.5 mL). The test tube was sealed and the reaction mixture was stirred at 110° C. for 28 h. The resulting suspension was cooled to room temperature and filtered through a 0.5×1 cm pad of silica gel, eluting with diethyl ether. The filtrate was concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (2×20 cm; pentane:diethyl ether 30:1) provided 139 mg (78% yield) of the title compound as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067955B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-d9bc3bcd3e734523874116f6f2861512 |
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| Source note | uspto-grants-2015_06 |
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