HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410332Generated: November 2, 2026
1-Bromo-2-methylpropane → HCID 69321934, compound
https://huagongshe.com/reaction/2410332
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | Isobutyl iodide | HCID 10556 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4H-1,3-Benzodioxin-4-one, 5-hydroxy-2,2-dimethyl- | HCID 11052514 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69321934 | HCID 69321934 | 82% |
Reaction Steps
A mixture of 5-hydroxy-2,2-dimethyl-4H-1,3-benzodioxin-4-one (880 mg, 4.53 mmol), potassium carbonate (1.89 g, 13.7 mmol) and isobutyl iodide (0.52 mL, 4.6 mmol) in N,N-dimethylformamide (5 mL) in a sealed tube was stirred at 80° C. After being stirred for 8 h, additional reagents (potassium carbonate: 2.0 g, 14 mmol; isobutyl bromide: 1.0 mL, 9.2 mmol) were added to the mixture, and the mixture was stirred at 130° C. for 10 h. After cooling to 80° C., methanol (3 mL) was added to the mixture, and the mixture was stirred further 15 h. Then the mixture was cooled to room temperature, diluted with ethyl acetate and washed with brine. The organic layer was dried over magnesium sulfate and concentrated in vacuo to give 836 mg (82%) of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08816090B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-0f789401e8294941b8744aaece9a9dec |
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| Source note | uspto-grants-2014_08 |
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