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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1214Generated: October 26, 2026

Benzoyl Peroxide → 4,6-Dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/1214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant6-Bromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthaleneHCID 10586063—
SolventCarbon TetrachlorideHCID 5943—
Product4,6-Dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthaleneHCID 19694961—

Reaction Steps

To a solution of 1.2 g (5.0 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene (Compound F) in 20 ml of CCl4 was added 0.97 g (5.5 mmol) of N-bromosuccinimide followed by 20 mg (0.08 mmol ) of benzoylperoxide. The mixture was refluxed for 3 hours, filtered and the filtrate washed with water (5 ml). The organic phase was dried over MgSO4 and then concentrated in vacuo to yield the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723620
Source datasetuspto-grants-1998_03
ORD IDord-d35af9b12f1b47e88a643494fdc123b8
Source noteuspto-grants-1998_03