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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222325Generated: November 1, 2026

Salicylaldehyde → 2-[(2-Methoxyethoxy)methoxy]benzaldehyde

https://huagongshe.com/reaction/2222325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
Product2-[(2-Methoxyethoxy)methoxy]benzaldehydeHCID 1968976171.6%

Reaction Steps

The hydroxyl group of 2-hydroxybenzaldehyde (3.0 g) was protected by use of 2-methoxyethoxymethyl chloride (3.1 g) in accordance with (production process 1), to thereby produce 2-methoxyethoxymethoxybenzaldehyde (3.7 g, yield: 70%). The thus-produced 2-methoxyethoxymethoxybenzaldehyde (2.0 g) and 3,4-dimethoxybenzyl cyanide (1.7 g) were subjected to condensation in accordance with process A of (production process 2), to thereby yield an MEM form of the target product. Subsequently, the protective group was removed from the MEM form in accordance with (production process 3), to thereby produce the target product (1.4 g, yield: 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371773B2
Source datasetuspto-grants-2008_05
ORD IDord-f252ae0f3be945edb1e44c4735ded78a
Source noteuspto-grants-2008_05