HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968971Generated: October 29, 2026
3-Chloro-2-methyl-1-propene → 1-Chloro-2-fluoro-4-(2-methylprop-2-en-1-yl)benzene
https://huagongshe.com/reaction/968971
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Bromo-1-chloro-2-fluorobenzene | HCID 2724690 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | Iodine | HCID 807 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Chloro-2-fluoro-4-(2-methylprop-2-en-1-yl)benzene | HCID 23109556 | — |
Reaction Steps
Magnesium (2.43 g) and iodine (10 mg) were added to tetrahydrofuran (40 ml) and a solution of 4-bromo-1-chloro-2-fluorobenzene (21.0 g) in tetrahydrofuran (40 ml) was added dropwise, and the mixture was stirred at room temperature for 1 hr to give a Grignard's reagent. The reaction mixture was ice-cooled and copper iodide (1.90 g) was added. 3-Chloro-2-methyl-1-propene (14.8 ml) was added and the mixture was stirred at room temperature for 1 hr. The reaction mixture was ice-cooled and saturated aqueous ammonium chloride solution (10 ml) was added. The mixture was stirred at room temperature for 20 min and magnesium sulfate (40 g) was added. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. Hexane (100 ml) was added to the obtained residue and insoluble materials were filtered off. The resulting solution was concentrated under reduced pressure to give the title compound (16.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07304174B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-2c244ac55eec4504814a6f9824bcfb52 |
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| Source note | uspto-grants-2007_12 |
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