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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180158Generated: October 26, 2026

6-Methoxy-2-(4-nitrophenyl)-1-[4-(phenylmethoxy)benzyl]-1,2,3,4-tetrahydroisoquinoline → 2-(4-Aminophenyl)-6-methoxy-1-[4-(phenylmethoxy)benzyl]-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/1180158

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-2-(4-nitrophenyl)-1-[4-(phenylmethoxy)benzyl]-1,2,3,4-tetrahydroisoquinolineHCID 23440823—
ReactantTin dichloride dihydrateHCID 43835034—
SolventWaterHCID 962—
SolventAcetic acid tetrahydrofuranHCID 23444217—
Product2-(4-Aminophenyl)-6-methoxy-1-[4-(phenylmethoxy)benzyl]-1,2,3,4-tetrahydroisoquinolineHCID 2344074995.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of 6-methoxy-2-(4-nitrophenyl)-1-[4-(phenylmethoxy)benzyl]-1,2,3,4-tetrahydroisoquinoline (0.70 g, 1.46 mmol) and SnCl2.H2O (1.35 g, 6.0 mmol) in 20 mL of THF/HOAc (1:1) and 3 mL of water was heated at 60° C. for 3 h. The reaction mixture was concentrated under reduced pressure and the resulting residue was quenched by the addition of saturated aqueous NaHCO3 (50 mL). The aqueous layer was extracted with EtOAc (3×50 mL) and the combined organic layer was dried over MgSO4 then concentrated. The crude product was purified by flash chromatography to provide the title compound (0.63 g, 95% yield). ES-MS, (m/z) 451 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279489B2
Source datasetuspto-grants-2007_10
ORD IDord-f76a998ea2474806bac45997088f47ad
Source noteuspto-grants-2007_10