HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423074Generated: November 2, 2026
Dimethylformamide → 2-Bromo-3,6-difluorobenzaldehyde
https://huagongshe.com/reaction/2423074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 2-Bromo-1,4-difluorobenzene | HCID 67862 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-3,6-difluorobenzaldehyde | HCID 50998399 | 73.8% |
Reaction Steps
To solution of diisopropylamine (13.29 mL, 93 mmol) in THF (300 mL) at −78° C., was added n-butyllithium (34.2 mL of 2.5M in hexanes, 85 mmol), dropwise over 10 mins. The mixture was stirred at −78° C. for 15 mins and then 2-bromo-1,4-difluorobenzene (15 g, 78 mmol) in THF (100 mL) was added dropwise over 15 mins maintaining the temperature below −65° C. After stirring for 1 hr at −78° C., N,N-dimethylformamide (6.62 mL, 85 mmol) was added via syringe. The mixture was stirred at −78° C. for 30 mins and then quenched with sat. NH4Cl solution and the mixture was allowed to reach room temperature. The product was extracted into ether and the extracts were dried (Na2SO4) and evaporated. Chromatography (silica, 0-100% dichloromethane in hexane) gave the title compound (D14) as a yellow solid (12.73 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960563B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-41af9c58072c451580d0cd65825695ec |
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| Source note | uspto-grants-2011_06 |
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