HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024007Generated: October 28, 2026
Dimethylformamide → 2,6-Dibromo-4-fluorobenzaldehyde
https://huagongshe.com/reaction/1024007
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,3-Dibromo-5-fluoro-2-iodobenzene | HCID 2724606 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,6-Dibromo-4-fluorobenzaldehyde | HCID 44474666 | 54% |
Reaction Steps
To a solution of 1,3-dibromo-5-fluoro-2-iodobenzene (50 g, 132 mmol) in anhydrous toluene (300 mL) cooled at −35° C. was added the solution of isopropylmagnesium chloride (84 mL, 171 mmol, 2.0M in Et2O) over 30 minutes while maintaining the internal temperature below −25° C. A clear brown solution was obtained and the stirring was continued for 1.5 h at −25° C. Then anhydrous DMF (34 mL, 436 mmol) was added over a period of 30 minutes. The reaction mixture was warmed to 10° C. (room temperature) over 1 h and stirred at this temperature for 1.5 h. It was then quenched with 3.0M HCl and followed by the addition of ethyl acetate. The organic layer was separated and evaporated under reduced pressure. The residue was purified by silica-gel column chromatography eluting with petroleum ether/ethyl acetate (from 50:1 to 20:1) to give 101h as a white solid (20 g, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722676B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-bfd60920e089440a97a5207531d0ae4c |
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| Source note | uspto-grants-2014_05 |
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