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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant1,2-Dibromo-5-chloro-3-fluorobenzeneHCID 2724907—
ReactantHCID 178418918HCID 178418918—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHeptaneHCID 8900—
Product2-Bromo-4-chloro-6-fluorobenzaldehydeHCID 7070118395%

Reaction Conditions

Temperature-45 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912221B2
Source datasetuspto-grants-2014_12
ORD IDord-fbde38cdab584307a010248ff9c37630
Source noteuspto-grants-2014_12