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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847187Generated: November 2, 2026

Iodobenzene → 5-phenoxy-3,4-dihydronaphthalen-1(2H)-one

https://huagongshe.com/reaction/1847187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodobenzeneHCID 11575—
ReactantSodium hydrideHCID 24758—
ReactantEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
Reactant5-Hydroxy-1-tetraloneHCID 119921—
CatalystCuprous chlorideHCID 62652—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-phenoxy-3,4-dihydronaphthalen-1(2H)-oneHCID 1072862518%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 5-hydroxy-1-tetralone (4.5 g, 28.0 mmol) and iodobenzene (24.0 g, 168.0 mmol) in DMF (50 mL) was added NaH (1.2 g, 30.0 mmol) at room temperature. The mixture was heated to 50° C. until the solid was dissolved and then cooled. To the mixture was added CuCl (2.8 g, 28.0 mmol); followed by tris(dioxa 3,6-heptyl)amine (2.7 g, 8.4 mmol). The mixture was heated at 145° C. overnight. The reaction was diluted with water, extracted with EtOAc, washed with brine, dried (Na2SO4), and concentrated. Purification by silica gel chromatography (20:1 PE/EtOAc) gave 1.2 g (18%) of the title compound as a yellow oil. [M+H] calc'd for C16H14O2, 239. Found 239.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952151B2
Source datasetuspto-grants-2015_02
ORD IDord-8ff5dc5186c049c1b25b6d8c8c39a8a2
Source noteuspto-grants-2015_02