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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403860Generated: October 26, 2026

Benzoyl Peroxide → Methyl 3-(bromomethyl)-4'-nitrobiphenyl-4-carboxylate

https://huagongshe.com/reaction/403860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 3-methyl-4'-nitrobiphenyl-4-carboxylateHCID 59385226—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 3-(bromomethyl)-4'-nitrobiphenyl-4-carboxylateHCID 67305902—

Reaction Conditions

Temperature80 °C

Reaction Steps

The compound of example 220 (5 g, 0.0184 mol) was dissolved in carbon tetrachloride (125 mL). Benzoyl peroxide (250 mg) and NBS (3.6 g, 0.0202 mol) were added and the reaction mixture was refluxed at 80° C. The reaction mixture was cooled to room temperature and filtered through celite. The filtrate was concentrated to yield crude residue containing 85% mono bromo and 10% dibromo product and 5% starting material. The crude title compound obtained was used directly for preparation of compound of example 222.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748426B2
Source datasetuspto-grants-2014_06
ORD IDord-a6f066b724b1453785be9275f7a10f9e
Source noteuspto-grants-2014_06