HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973043Generated: October 30, 2026
Hydrochloric Acid → HCID 21403372, compound
https://huagongshe.com/reaction/973043
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 12707063 | HCID 12707063 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | HCID 178418361 | HCID 178418361 | — |
| Product | HCID 21403372 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04054659 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-15114816061a4ba4858e5eac3ab30735 |
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| Source note | uspto-grants-1977_10 |
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