HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935558Generated: October 25, 2026
Diisopropylamine → 1-Bromo-3-chloro-2,4-difluorobenzene
https://huagongshe.com/reaction/1935558
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Hexachloroacetone | HCID 8303 | — |
| Reactant | 1-Bromo-2,4-difluorobenzene | HCID 67674 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Bromo-3-chloro-2,4-difluorobenzene | HCID 2773256 | — |
Reaction Steps
To a solution of 19 ml (0.135 mole) of diisopropylamine in 125 ml of tetrahydrofuran (THF) cooled at −20° C. is added 80 ml of n-butyllithium (1.6 M in hexane). The temperature is raised to 0° C. for 5 minutes and lowered to −78° C. Then 25 g (0.129 mole) of 2,4-difluoro-bromobenzene is then added and the reaction is stirred at −65° C. for 2 hours. Then, 25 ml (0.164 mole) of hexachloroacetone is added and the solution is warmed at room temperature. After evaporation of the solvent, the residue is distilled under vacuum to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06387928B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-e8276d98556848c5bbe4110e2f9a6dd7 |
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| Source note | uspto-grants-2002_05 |
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