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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655651Generated: October 25, 2026

Chloromethyl Methyl Ether → 5-Bromo-3-methoxy-2-(methoxymethoxy)benzaldehyde

https://huagongshe.com/reaction/655651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromo-2-hydroxy-3-methoxybenzaldehydeHCID 262238—
SolventDichloromethaneHCID 6344—
Product5-Bromo-3-methoxy-2-(methoxymethoxy)benzaldehydeHCID 11565322106.8%

Reaction Steps

Ethyldiisopropylamine (3.01 ml, 17.1 mmol) and methoxymethylchloride (1.5 ml, 15.7 mmol) were added to a dichloromethane solution (30 ml) of 5-bromo-2-hydroxy-3-methoxybenzaldehyde (3.3 g, 14.3 mmol) under ice cooling, and the mixture was stirred at room temperature for 2 hours. The reaction solution was washed with water, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1→11:9). The purified product was concentrated to dryness under reduced pressure to obtain 5-bromo-3-methoxy-2-methoxymethoxybenzaldehyde (4.2 g) as light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071600B2
Source datasetuspto-grants-2011_12
ORD IDord-6cb00748a0a0469c8784194f0d1e935e
Source noteuspto-grants-2011_12