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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantNeopentyl alcoholHCID 6404—
ReactantCesium carbonateHCID 10796—
Reactant2-Bromo-1-iodo-3-methylbenzeneHCID 50998158—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
Product2-Bromo-1-methyl-3-(neopentyloxy)benzeneHCID 67325713—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-9b910a8d104a44dda92de3b12f1c731f
Source noteuspto-grants-2014_05