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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597206Generated: October 31, 2026

3,4-Dihydro-6-methoxy-5-(phenylmethoxy)-2(1H)-isoquinolinecarboxaldehyde → HCID 21446991, compound

https://huagongshe.com/reaction/597206

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dihydro-6-methoxy-5-(phenylmethoxy)-2(1H)-isoquinolinecarboxaldehydeHCID 21447037—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 21446991HCID 2144699192%

Reaction Steps

89.2 g of 5-benzyloxy-2-formyl-1,2,3,4-tetrahydro-6-methoxy-isoquinoline are dissolved in 450 ml of glacial acetic acid and hydrogenated at room temperature and normal pressure in the presence of 4.5 g of 5 percent palladium black. After conclusion of hydrogen absorption, the reaction mixture is separated from the catalyst by filtration and evaporated to dryness under reduced pressure. Recrystallization of the residue from ethanol gives 57.2 g of 2-formyl-1,2,3,4-tetrahydro-5-hydroxy-6-methoxy-isoquinoline. m.p. = 172.5° - 173.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04013663
Source datasetuspto-grants-1977_03
ORD IDord-0840521759c84c31aff50d2e2ba013ab
Source noteuspto-grants-1977_03