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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109348Generated: October 30, 2026

Water → 2-(Methoxymethoxy)-4-(phenylmethoxy)benzaldehyde

https://huagongshe.com/reaction/2109348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Benzyloxy-2-hydroxybenzaldehydeHCID 561235—
SolventDichloromethaneHCID 6344—
Product2-(Methoxymethoxy)-4-(phenylmethoxy)benzaldehydeHCID 1786206079%

Reaction Steps

To a solution of 4-benzyloxy-2-hydoxy-benzaldehyde (44.9 g, 197 mmol) synthesized in step (a) of Example 197 in dichloromethane (200 ml) were added diisopropylethylamine (52.0 ml, 300 mmol) and methoxymethyl chloride (20.5 ml, 270 mmol) at 0° C. with stirring, and the resulting mixture was stirred overnight at room temperature under a nitrogen atmosphere. After stirring, water (200 ml) was added, and the resulting mixture was extracted with dichloromethane (200 ml×2). The organic layer was washed successively with water (300 ml×1) and saturated aqueous sodium chloride solution (300 ml×1), dried over anhydrous sodium sulfate, filtered, and evaporated in vacuo to afford the crude product. The crude product was purified by chromatography on a silica gel column using a mixed solvent of hexane and ethyl acetate (5:1-1:1) as the eluent to afford the title compound (42.2 g, yield: 79%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514475B2
Source datasetuspto-grants-2009_04
ORD IDord-d3195df1145e4c54ad6434a42ec5055a
Source noteuspto-grants-2009_04