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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622195Generated: November 2, 2026

Sulfuric Acid → N-(2-methoxy-3,4-methylenedioxybenzyl)-N-(p-toluenesulfonyl)aminoacetaldehyde diethylacetal

https://huagongshe.com/reaction/622195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13911324HCID 13911324—
ProductN-(2-methoxy-3,4-methylenedioxybenzyl)-N-(p-toluenesulfonyl)aminoacetaldehyde diethylacetalHCID 1391132578%

Reaction Conditions

Temperature5 °C

Reaction Steps

5.67 g (20 mmol) of N-(2-methoxy-3,4-methylenedioxybenzyl)-N-methylaminoacetaldehyde dimethylacetal (1) obtained in Example 3 was dissolved in 40 ml of 6N sulfuric acid. After stirring at 76°-7° C. for 1.5 hours, the reaction mixture was cooled and the pH was controlled to about 11 by adding 25% aqueous solution of sodium hydroxide at a temperature lower than 30° C. It was extracted with 35 ml and then 10 ml of methylene chloride successively, which were combined and washed with 20 ml of water and then dried over anhydrous magnesium sulfate. The solvent was concentrated under vacuum, the residue was dissolved under heating by adding 12 ml of ethanol and then cooled to 5° C. to deposit crystals. The crystals were collected by filtration, washed with 3 ml of cold ethanol and then dried under vacuum to obtain 3.71 g (yield 78%) of 4-hydroxy-8-methoxy-2-methyl-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline (2), m.p. 152°-3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04769480
Source datasetuspto-grants-1988_09
ORD IDord-97a73bd2c139415aab11090d0cbabd50
Source noteuspto-grants-1988_09