Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | 1,2-Benzenediol, 3-bromo- | HCID 26659 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromo-1,3-benzodioxole | HCID 2776189 | 45% |
Reaction Steps
To 2,3-dihydroxy-bromobenzene (3.0 g, 0.16 mole), KF (4.63 g, 0.080 mole), DMF (15 mL was added CH2Br2 (4.13 g, 0.024 moles). This suspension was heated to 135° C. for 3 hours, cooled and filtered. The filtrate was poured into 200 mL of ether and washed with water, 1 N KOH and brine. The organic layer was dried over magnesium sulfate, filtered and the solvent removed under vacuum, to yield 2,3-Methylenedioxy-bromobenzene (1.45 g, 45 % yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06342504B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-966e1995263f40bcb81f4af0d7c3253a |
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| Source note | uspto-grants-2002_01 |
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