HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407610Generated: October 30, 2026
Dimethylformamide → 2,6-Dibromo-4-fluorobenzaldehyde
https://huagongshe.com/reaction/407610
Participants
| Role | Name | HCID | Charge |
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| 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
A solution of 1,3-dibromo-5-fluoro-2-iodobenzene (50 g, 132 mmol) in anhydrous toluene (300 mL) cooled to −35° C. was added the solution of isopropylmagnesium chloride (84 mL, 171 mmol, 2.0 M in diethyl ether) over a period of 30 minutes while maintaining the internal temperature below −25° C. A clear brown solution was obtained. Stirring was continued for 1.5 h. Then anhydrous DMF (34 mL, 436 mmol) was added over a period of 30 minutes. The temperature of the reaction mixture increased to −19° C. The reaction mixture was warmed to 10° C. (room temperature) over 1 h and stirred at this temperature for 1.5 h. The reaction was quenched with saturated aqueous NH4Cl (100 mL), filtered 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 102a (20 g, yield 54%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754077B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-e10957b638ba4322a64d81faf679ece8 |
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| Source note | uspto-grants-2014_06 |
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