HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423078Generated: October 27, 2026
Dimethylformamide → 2-Bromo-3-chloro-6-fluorobenzaldehyde
https://huagongshe.com/reaction/2423078
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 2-Bromo-1-chloro-4-fluorobenzene | HCID 2773263 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-3-chloro-6-fluorobenzaldehyde | HCID 59272964 | 58.9% |
Reaction Steps
To a solution of diisopropylamine (5 mL, 35.4 mmol) in THF (30 mL) at 0° C. under argon was added n-butyl lithium (16.5 mL of 1.6 M solution in hexane, 26.4 mmol) slowly over 20 minutes. The mixture was cooled to −75° C. and 2-bromo-1-chloro-4-fluorobenzene (5 g, 23.9 mmol) in THF (20 mL) was added dropwise over 15 mins whilst maintaining the temperature <−70° C. The solution was then stirred at −75° C. for 45 mins and then DMF (2.2 mL, 28.6 mmol) was added over 5 mins. The mixture was stirred at −78° C. for 2 hrs and then allowed to reach room temperature. Water was added and the aqueous layer was extracted with ethyl acetate. The combined extracts were washed with brine and the solvent evaporated. Chromatography (silica gel, ethyl acetate/hexane) gave the title compound (D21) as a yellow solid (3.344 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-7284bce253ed4c6c9d3e4ae04b4f575c |
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| Source note | uspto-grants-2011_06 |
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