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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100358Generated: November 1, 2026

Hydrochloric Acid → 1-Bromo-3,5-dichloro-2-methoxybenzene

https://huagongshe.com/reaction/2100358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-4,6-dichlorophenolHCID 20617—
SolventAcetoneHCID 180—
Product1-Bromo-3,5-dichloro-2-methoxybenzeneHCID 17087326113.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Bromo-4,6-dichlorophenol (Preparation 24, 4.6 g, 19 mmol), potassium carbonate (4.5 g, 32.3 mmol) and methyl iodide (1.8 ml, 20.5 mmol) were combined in 46 ml acetone and heated to reflux for 18 hours. The reaction was cooled to 0° C., 1N HCl (aqueous) was added to give pH 3, and the reaction was extracted into 50 ml ethyl acetate. The organic layer was washed with brine (2×20 ml), dried over sodium sulphate and concentrated in vacuo to afford the title compound as a brown solid (5.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572797B2
Source datasetuspto-grants-2009_08
ORD IDord-e270c987cee64043a33661ecb3fdd6d6
Source noteuspto-grants-2009_08