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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622203Generated: October 31, 2026

Hydrochloric Acid → 2-Methoxy-3,4-methylenedioxybenzylalcohol

https://huagongshe.com/reaction/622203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2-DimethoxyethylmethylamineHCID 8503—
Reactant1,3-Benzodioxole-5-carboxaldehyde, 4-methoxy-HCID 10197946—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-Methoxy-3,4-methylenedioxybenzylalcoholHCID 1528723711%
Product2-Methoxy-3,4-methylenedioxytolueneHCID 212940062%

Reaction Steps

To 100 ml of ethanol, were charged 0.9 ml of ethanol containing 22.2 g of hydrochloric acid dissolved therein, 1.98 g of N-methylaminoacetaldehyde dimethylacetal, 1.0 g of 2-methoxy-3,4-methylenedioxybenzaldehyde, 10 ml of ethanol and 0.12 g of 5% palladium on carbon catalyst and hydrogenation was carried out at room temperature. The reaction was completed in 3 hours. The amount of hydrogen absorption was 103% of the theoretical amount. After the reaction was over, the catalyst was filtered out and 2N NaOH aqueous solution was added to the reaction mixture to make the filtrate alkaline (pH 11). The resulting mixture was then extracted with ethyl acetate. The liquid extract was analyzed by GC and LC to show 1.29 g of 2-methoxy-3,4-methylenedioxy-N-methylbenzylamino dimethylacetal (yield 82%), 0.11 g of 2-methoxy-3,4-methylenedioxybenzylalcohol (yield 11%) and 0.02 mg of 2-methoxy-3,4-methylenedioxy toluene (yield 2%), while 2-methoxy-3,4-methylenedioxybenzaldehyde of the starting material not being recognized (conversion rate:100%). The selectivity to the desired 2-methoxy-3,4-methylenedioxy-N-methylbenzylamino dimethylacetal was 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04769480
Source datasetuspto-grants-1988_09
ORD IDord-08b601c796a94ac780155740f55491fa
Source noteuspto-grants-1988_09