HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719040Generated: October 29, 2026
Dimethylformamide → 4-Bromo-2,5-dimethylbenzaldehyde
https://huagongshe.com/reaction/719040
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzene, 1,4-dibromo-2,5-dimethyl- | HCID 66175 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 4-Bromo-2,5-dimethylbenzaldehyde | HCID 13119101 | 40% |
Reaction Steps
4 g (15 mmol, 1 eq.) of 1,4-dibromo-2,5-dimethylbenzene are solubilized in 50 mL of distilled THF, in a Schlenk tube under argon. The medium is then cooled to −78° C., then 6.6 mL (16.6 mmol, 1.1 eq.) of BuLi (2.5M in hexane) are added dropwise. After stirring at this temperature for 1 hour, 5.3 mL (68 mmol, 4.5 eq.) of freshly distilled DMF are added. The reaction medium is again stirred at this temperature for 1 hour, and then the temperature returns to ambient temperature overnight. Next, the medium is diluted with a solution of ammonium chloride and then extracted three times with ethyl acetate. The organic phases are combined, dried over magnesium sulphate, and concentrated under reduced pressure. The residue is purified by silica column chromatography (eluent: ethyl acetate/petroleum ether: 80/20), so as to give a white solid (m: 1.3 g, yield: 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09196847B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-64e31ead7aa2496cb1ada202bf8f9901 |
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| Source note | uspto-grants-2015_11 |
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