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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845829Generated: October 29, 2026

Sodium Hydroxide → HCID 13912214, compound

https://huagongshe.com/reaction/845829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,2-Diethoxy-N-((4-methoxybenzo[D][1,3]dioxol-5-YL)methyl)-N-methylethan-1-amineHCID 13912213—
SolventSulfuric AcidHCID 1118—
ProductHCID 13912214HCID 1391221480.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

62.29 g (0.2 mol) of N-(2-methoxy-3,4-methylenedioxybenzyl)-N-methylaminoacetaldehyde diethylacetal (3) was dissolved in 400 ml of 6N sulfuric acid and the solution was stirred under heating at 76°-78° C. for 1.5 hour. The solution was cooled and added with 25% aqueous solution of sodium hydroxide at a temperature below 30° C. to make the pH of the solution about 11. Then the solution was extracted with 200 ml and then with 100 ml of methylene chloride successively. The extracts were joined, washed with 100 ml of water and then dried over anhydrous mgnesium sulfate. The salt was filtered out and the magnesium was concentrated under reduced pressure. The residue was added with 120 ml of ethanol and dissolved by heating. Then, the solution was cooled to 5° C. to be crystalized. These crystals are filtered out, washed with 30 ml of cold ethanol and dried under a reduced pressure to obtain 38.09 g of 4-hydroxy- 8-methoxy-2-methyl-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline (m.p. 151°-153° C., yield: 80.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04760145
Source datasetuspto-grants-1988_07
ORD IDord-a4981ea681cc4b0b883749040c0c7b0d
Source noteuspto-grants-1988_07