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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708129Generated: October 30, 2026

7-Bromo-1,2,3,4-tetrahydronaphthalen-1-one → HCID 18960968, compound

https://huagongshe.com/reaction/1708129

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Bromo-1,2,3,4-tetrahydronaphthalen-1-oneHCID 252731—
ReactantSodium pentafluoropropionateHCID 2733305—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 18960968HCID 1896096880%

Reaction Steps

To a solution of 10 g (0.044 mol) of 7-bromo-1,2,3,4-tetrahydronaphthalenone in 300 mL of N-methylpyrrolidone was added 32.23 g (0.17 mol) of CuI and 31.59 g (0.17 mol) of sodium pentafluoropropanoate and the mixture was heated for 3 h at reflux under an argon atmosphere. After cooling to room temperature, the resulting suspension was poured into a mixture of H2O--Et2O (1:1) and filtered over celite. The layers were separated and the organic phase was washed with H2O and dried over MgSO4. The solvent was removed, to afford a residue that was chromatographed on silica gel (hexane-AcOEt), to give the desired product as a colourless oil (8.75 g, yield: 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356915
Source datasetuspto-grants-1994_10
ORD IDord-aa0504312d864e5b9b58d58be25e9cb3
Source noteuspto-grants-1994_10