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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097461Generated: October 30, 2026

Hydrochloric Acid → 5-Bromo-2-(methoxymethoxy)benzaldehyde

https://huagongshe.com/reaction/2097461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium CarbonateHCID 11430—
Reactant5-BromosalicylaldehydeHCID 72863—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product5-Bromo-2-(methoxymethoxy)benzaldehydeHCID 1970162677.3%

Reaction Steps

To 600 ml of acetone solution containing 30.0 g (0.15 mol) of 5-bromo-2-hydroxybenzaldehyde was added 20.6 g (0.15 mol) of potassium carbonate, and then, 12.5 ml (0.17 mol) of chloromethylmethyl ether was added dropwise to the mixture over 30 minutes under ice-cooling. After stirring the mixture at the same temperature for 30 minutes, the mixture was further stirred at room temperature for 5 hours. After completion of the reaction, 600 ml of water was added to the reaction mixture. A pH of the mixture was adjusted to 7.6 with conc. hydrochloric acid, and extracted with ethyl acetate. The organic layer after separation was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 28.4 g of the title compound as a pale yellowish oil. (Yield: 77%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450319B2
Source datasetuspto-grants-2013_05
ORD IDord-d6b13c38416d40baa3447b7f442b91b5
Source noteuspto-grants-2013_05