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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443144Generated: October 25, 2026

Potassium Carbonate → 1-(Chloromethyl)-2-fluoro-3-methoxybenzene

https://huagongshe.com/reaction/1443144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Fluoro-3-methoxybenzyl alcoholHCID 593589—
SolventDichloromethaneHCID 6344—
Solventtert-Butyl methyl etherHCID 15413—
Product1-(Chloromethyl)-2-fluoro-3-methoxybenzeneHCID 53870833—

Reaction Steps

24.79 g (158.75 mmol) of 2-fluoro-3-methoxybenzyl alcohol is dissolved in 35 ml of dichloromethane. While being cooled slightly, 58.4 ml of thionyl chloride is added in drops, and the batch is then stirred overnight at room temperature. The reaction mixture is spun in until a dry state is reached, the residue is dissolved in methyl tert-butyl ether, and it is shaken twice with semi-saturated potassium carbonate solution. The aqueous phase is extracted once with methyl tert-butyl ether. The combined organic extracts are worked up as usual. The residue that is obtained is incorporated in crude form into the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659297B2
Source datasetuspto-grants-2010_02
ORD IDord-a9a6b7605c444130a32f61aeeae913c6
Source noteuspto-grants-2010_02