HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572407Generated: October 25, 2026
Dimethylformamide → 4-Bromo-2,5-difluorobenzaldehyde
https://huagongshe.com/reaction/572407
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1,4-Dibromo-2,5-difluorobenzene | HCID 67596 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Bromo-2,5-difluorobenzaldehyde | HCID 22489081 | 37% |
Reaction Steps
n-Butyl lithium (3.6 ml, 7.7 mmol) was added drop wise to a solution of 1,4-dibromo-2,5-difluoro-benzene (2 g, 7.35 mmol) in dry ether at −78° C. under nitrogen atmosphere and the resulting mixture was stirred at −78° C. for 30 minutes. This was followed by the addition of DMF (0.85 ml, 11.03 mmol) in dry THF. The resultant was stirred at room temperature for 1 hour. The reaction was monitored by TLC (5% ethyl acetate in hexane). The reaction mixture was partitioned between ethyl acetate and saturated ammonium chloride. The organic layer was concentrated and purified by column chromatography on silica gel (2% ethyl acetate in hexane) to afford 600 mg of the product (37% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029399B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-5f194aae72294b5c9d42b853a801076a |
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| Source note | uspto-grants-2015_05 |
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