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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012665Generated: November 1, 2026

4-Bromo-2-chloro-1-iodobenzene → HCID 67313561, compound

https://huagongshe.com/reaction/1012665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-chloro-1-iodobenzeneHCID 2735547—
Reactant2-Chloro-5-methoxybenzaldehydeHCID 12927838—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67313561HCID 67313561—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of 4-bromo-2-chloro-1-iodo-benzene (10.0 g, 31.5 mmol) in THF (120 ml) was added 2 M solution of isopropylmagnesium chloride in THF (17.3 ml, 34.60 mmol) at −65° C. The reaction mixture was stirred at −40° C. for 20 min. After 2-chloro-5-methoxy-benzaldehyde (5.5 g, 32.20 mmol) was added, the reaction mixture was warmed to room temperature and stirred overnight. Then the solution was quenched with saturated aqueous solution of NH4Cl. The aqueous phase was extracted twice with diethyl ether. The combined organic phases were dried over MgSO4 and concentrated in vacuo. The crude material was purified by chromatography (petroleum ether/CH2Cl2 1:1) to provide title compound as a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977387B2
Source datasetuspto-grants-2011_07
ORD IDord-cf95ca44ea03494d8189001044ecf14b
Source noteuspto-grants-2011_07