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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304648Generated: November 1, 2026

6-Methoxy-2-(methylethyl)-1-[4-(phenylmethoxy)benzyl]-1,2,3,4-tetrahydroisoquinoline → 6-Methoxy-2-(methylethyl)-1-(4-hydroxybenzyl)-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/2304648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-2-(methylethyl)-1-[4-(phenylmethoxy)benzyl]-1,2,3,4-tetrahydroisoquinolineHCID 23440839—
CatalystAcetic AcidHCID 176—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product6-Methoxy-2-(methylethyl)-1-(4-hydroxybenzyl)-1,2,3,4-tetrahydroisoquinolineHCID 2344073791%

Reaction Steps

A suspension of 6-methoxy-2-(methylethyl)-1-[4-(phenylmethoxy)benzyl]-1,2,3,4-tetrahydroisoquinoline (0.3 g, 0.75 mmol), palladium (10% wt) on activated carbon (0.06 g) and acetic acid (5 drops) in ethyl acetate (10 mL) was stirred under hydrogen overnight. The reaction was filtered and concentrated to provide the title compound (0.212 g, 91% yield): ES-MS (m/z) 312 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06436923B1
Source datasetuspto-grants-2002_08
ORD IDord-2322180a350b44ceb141524c3d3b3a84
Source noteuspto-grants-2002_08