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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106025Generated: October 31, 2026

2-(3-Bromophenyl)-1,3-dioxane → 4-(3-[1,3]Dioxan-2-ylphenyl)-1,1,1-trifluoro-4-methylpentan-2-one

https://huagongshe.com/reaction/2106025

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Bromophenyl)-1,3-dioxaneHCID 10105815—
Reactant1,1,1-Trifluoro-4-methylpent-3-en-2-oneHCID 22032691—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Product4-(3-[1,3]Dioxan-2-ylphenyl)-1,1,1-trifluoro-4-methylpentan-2-oneHCID 57809966—

Reaction Steps

To a solution of the Grignard reagent derived from 2-(3-bromophenyl)-[1,3]dioxane (52.6 mL of 0.25M in THF, 13.1 mmol) at 0° C. was added copper (I) iodide (25 g, 13.1 mmol). After 45 minutes, 1,1,1-trifluoro-4-methylpent-3-en-2-one (2 g, 13.1 mmol) was added and the reaction mixture slowly warmed to room temperature and stirred overnight. The mixture was quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The combined organic layers were washed with saturated aqueous sodium chloride solution, dried with sodium sulfate, and concentrated in vacuo. The residue was triturated with hexanes and filtered. The filtrate was concentrated in vacuo to give 4-(3-[1,3]dioxan-2-ylphenyl)-1,1,1-trifluoro-4-methylpentan-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579469B2
Source datasetuspto-grants-2009_08
ORD IDord-378125540864487582fd5ce401f22e0b
Source noteuspto-grants-2009_08