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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Dimethyl-5-(1-methylethylidene)-1,3-dioxane-4,6-dione | HCID 75218 | — |
| Reactant | 4-Bromo-2-fluoro-1-iodobenzene | HCID 2724516 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118622760 | HCID 118622760 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365520B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-63b395776f9e42fa9e00864cf2f96fb1 |
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| Source note | uspto-grants-2016_06 |
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