HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49188Generated: October 25, 2026
Dimethylformamide → 5-Fluoro-2-methylbenzaldehyde
https://huagongshe.com/reaction/49188
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Bromo-4-fluorotoluene | HCID 74016 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-Fluoro-2-methylbenzaldehyde | HCID 2759012 | 98.4% |
Reaction Steps
A solution of 2-bromo-4-fluorotoluene (16.0 g) in anhydrous tetrahydrofuran was treated dropwise at −78° C. with a 1.6 M solution of butyllithium in hexane (55.5 ml). At the same temperature, the mixture was stirred and treated dropwise with a solution of dimethylformamide (6.8 g) in tetrahydrofuran (20 ml). After being allowed to warm to 0° C., the reaction mixture was combined with ice-water. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed successively with water and saturated brine, and then dried over magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 5-fluoro-2-methylbenzaldehyde (11.5 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706732B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-6b78eb3c3e5c4060a7cb232406f7f67d |
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| Source note | uspto-grants-2004_03 |
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