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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973043Generated: October 30, 2026

Hydrochloric Acid → HCID 21403372, compound

https://huagongshe.com/reaction/973043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantHCID 12707063HCID 12707063—
ReactantEthanol hydrochlorideHCID 21887872—
CatalystAdams' catalystHCID 345198—
SolventHCID 178418361HCID 178418361—
ProductHCID 21403372HCID 21403372—

Reaction Steps

A mixture of 1.4 g of 5,7-dibenzyloxy-1-(3,4,5-trimethoxybenzyl)-isoquinoline, 0.7 g of platinum dioxide, 100 ml of a hydrochloric acid-ethanol solution (the content of hydrochloric acid: 9%) and 50 ml of ethanol is shaken at 25° C in hydrogen atmosphere. After 150 ml of hydrogen are absorbed, the catalyst is removed by filtration. The filtrate is evaporated to remove solvent, whereby a mixture of 5,7-dihydroxy-1-(3,4,5-trimethoxybenzyl)-isoquinoline hydrochloride and 5,7-dihydroxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline hydrochloride is obtained. This mixture is recrystallized 33 times from ethanol, whereby 0.3 g of 5,7-dihydroxy-1-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydrolsoquinoline hydrochloride is obtained. Yield: 40% The physiocochemical properties of this product are identical with those of the compound obtained in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04054659
Source datasetuspto-grants-1977_10
ORD IDord-15114816061a4ba4858e5eac3ab30735
Source noteuspto-grants-1977_10