HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819497Generated: November 3, 2026
Dimethylformamide → 4-Bromo-2,6-difluorobenzaldehyde
https://huagongshe.com/reaction/1819497
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Bromo-3,5-difluorobenzene | HCID 136313 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Bromo-2,6-difluorobenzaldehyde | HCID 2773290 | — |
Reaction Steps
To a THF (250 mL) solution of diisopropylamine (53 mL) was added 2.44 M hexane solution of butyl lithium at −78° C., and the reaction mixture was stirred for 30 miniute. To the reaction mixture was added a THF solution of 3,5-difluorobromobenzene (1) (36 g), and then the reaction mixture was stirred for 1 h. To the reaction mixture was added DMF 146 mL, and the reaction mixture was stirred for additional 1 h. To the reaction mixture was added a saturated ammonium chloride aqueous solution, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate=20:1) to obtain the compoumd (2) 23.2 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601746B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-fd3f069efc494c0f825e9a149babd938 |
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| Source note | uspto-grants-2009_10 |
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