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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202225Generated: November 1, 2026

2,2-Dimethyl-5-(1-methylethylidene)-1,3-dioxane-4,6-dione → HCID 118622760, compound

https://huagongshe.com/reaction/2202225

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Dimethyl-5-(1-methylethylidene)-1,3-dioxane-4,6-dioneHCID 75218—
Reactant4-Bromo-2-fluoro-1-iodobenzeneHCID 2724516—
ReactantHCID 178418918HCID 178418918—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118622760HCID 118622760—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution (183 mL, 182.79 mmol) of 1M isopropylmagnesium chloride in THF was added dropwise to a solution of 4-bromo-2-fluoro-1-iodobenzene (50.0 g, 166.17 mmol) in anhydrous THF (96 mL) over 20 min at −20° C. under argon atmosphere. The reaction mixture was stirred at −20° C. for 30 min, and added dropwise to a solution of 5-isopropylidene-2,2-dimethyl-1,3-dioxane-4,6-dione in anhydrous toluene (84 mL) over 20 min at −20° C., and then the used container was washed with THF (24 mL). The reaction mixture was stirred at 0° C. for 3 hr, 10% aqueous citric acid solution (200 mL) was added thereto at 0° C., and the mixture was extracted with toluene (200 mL). The organic layer was concentrated under reduced pressure to give 5-(2-(4-bromo-2-fluorophenyl)propan-2-yl)-2,2-dimethyl-1,3-dioxane-4,6-dione as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365520B2
Source datasetuspto-grants-2016_06
ORD IDord-63b395776f9e42fa9e00864cf2f96fb1
Source noteuspto-grants-2016_06