HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404553Generated: October 30, 2026
Hydrochloric Acid → 2-Bromo-4-chloro-6-fluorobenzaldehyde
https://huagongshe.com/reaction/1404553
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,2-Dibromo-5-chloro-3-fluorobenzene | HCID 2724907 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 2-Bromo-4-chloro-6-fluorobenzaldehyde | HCID 70701183 | 95% |
Reaction Steps
To a solution of 1,2-dibromo-5-chloro-3-fluoro-benzene (10 g, 34.68 mmol) in heptane (27 ml) was added THF (44 ml) and the mixture was cooled to −45° C. Then iPrMgCl (38.14 ml, 38.14 mmol, 1M solution in THF) was added dropwise to the reaction mixture maintaining the temperature between −40° C. to −45° C. The mixture was stirred for 30 minutes at −40° C. before DMF (13.4 ml, 173.4 mmol) was added dropwise to the reaction mixture maintaining the temperature between −45° C. to −20° C. After stirring for another 15 minutes at −20° C., the reaction mixture was poured into a mixture of 2N HCl (20 ml) and ether (50 ml) at 0° C. The organic layer was separated and the aqueous layer was extracted two times with ether. The combined organic layers were dried with Na2SO4 and evaporated in vacuo to obtain the title compound as yellow solid (7.8 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912221B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-fbde38cdab584307a010248ff9c37630 |
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| Source note | uspto-grants-2014_12 |
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