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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235629Generated: October 30, 2026

Benzoyl Peroxide → HCID 59218436, compound

https://huagongshe.com/reaction/2235629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 57835884HCID 57835884—
ReactantHCID 59300572HCID 59300572—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 59218436HCID 59218436—

Reaction Steps

6-(Bromomethyl)-4,4-diethyl-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene (44.2) Starting material 44.1 was prepared according to the published procedure of Kim, C. et al. (Tetrahedron. Lett. 1994, 35 (19), 3017-3020). A mixture of 44.1 (0.5 g, 2.17 mmol), NBS (0.58 g, 3.25 mmol), and dibenzoyl peroxide (53 mg) in CCl4 (10 mL) was heated at reflux for 5 hours. The reaction was cooled, and the precipitate was filtered out. The solvent was removed providing crude 44.2, which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714008B2
Source datasetuspto-grants-2010_05
ORD IDord-5cadc8c0454e408dafb8e3839dd88f0a
Source noteuspto-grants-2010_05