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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460392Generated: October 25, 2026

2-Methoxybenzaldehyde → (2-Methoxyphenyl)(3-methyl-2-methoxymethoxyphenyl)methanol

https://huagongshe.com/reaction/1460392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxybenzaldehydeHCID 8658—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(Methoxymethoxy)-2-methylbenzeneHCID 3839351—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventN,N,N',N'-TetramethylethylenediamineHCID 8037—
SolventHexaneHCID 8058—
Product(2-Methoxyphenyl)(3-methyl-2-methoxymethoxyphenyl)methanolHCID 19812676137.2%

Reaction Steps

1-Methyl-2-methoxymethoxybenzene (15.2 g) was added to a mixture of 75 ml of a 1.6M solution of n-butyl lithium in hexane and 18.1 ml of tetramethylethylenediamine at 0° C. with stirring. After 4 hours, 13.6 g of o-anisaldehyde dissolved in 30 ml of tetrahydrofuran was added. The mixture was allowed to react for 0.5 hour and was then poured into a mixture of ice and saturated aqueous ammonium chloride. The resulting mixture was extracted with ether and the ether extract was dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain 39.5 g of the title compound as an off-white solid. The assigned structure was consistent with the proton NMR spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05071465
Source datasetuspto-grants-1991_12
ORD IDord-9405cc635e3c4ef996944285c3b2a2e4
Source noteuspto-grants-1991_12