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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750265Generated: October 31, 2026

2-benzyl-6-bromo-3-(1-hydroxyethyl)-4-phenyl-2H-isoquinolin-1-one → 3-acetyl-2-benzyl-6-bromo-4-phenyl-2H-isoquinolin-1-one

https://huagongshe.com/reaction/750265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-benzyl-6-bromo-3-(1-hydroxyethyl)-4-phenyl-2H-isoquinolin-1-oneHCID 23061004—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product3-acetyl-2-benzyl-6-bromo-4-phenyl-2H-isoquinolin-1-oneHCID 2306067260.3%

Reaction Steps

To a solution of 2-benzyl-6-bromo-3-(1-hydroxyethyl)-4-phenyl-2H-isoquinolin-1-one (250 mg) in THF (5 ml) was added manganese(IV) oxide (500 mg), and the mixture was heated under reflux for 1 hr. To the reaction mixture was add manganese(IV) oxide (500 mg) and the mixture was heated under reflux for 1 hr, manganese(IV) oxide (500 mg) was added and the mixture was heated under reflux for 1 hr, and manganese(IV) oxide (500 mg) was added and the mixture was heated under reflux for 12 hrs. The reaction mixture was filtered and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (hexane-hexane:ethyl acetate=8:1) and recrystallized (ethyl acetate-hexane) to give the title compound (150 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402595B2
Source datasetuspto-grants-2008_07
ORD IDord-d3ed62cbaa01469591e40e2ebb28bc3b
Source noteuspto-grants-2008_07