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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426139Generated: October 26, 2026

Benzoyl Peroxide → 4-(3-Bromomethyl-5-methyl-phenoxy)-2,6-dichloro-5-isopropyl-pyrimidine

https://huagongshe.com/reaction/426139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2,4-Dichloro-6-(3,5-dimethyl-phenoxy)-5-isopropyl-pyrimidineHCID 18925252—
CatalystTungstenHCID 23964—
SolventCarbon TetrachlorideHCID 5943—
Product4-(3-Bromomethyl-5-methyl-phenoxy)-2,6-dichloro-5-isopropyl-pyrimidineHCID 5918468966.2%

Reaction Steps

A mixture of (65) (9.72 g, 31 mmol), NBS (5.56 g, 31 mmol), and benzoyl peroxide (0.756 g, 3.1 mmol) in carbon tetrachloride (60 ml) was refluxed for 3 hr. under a light of 500 W tungsten lamp. After cooling to room temperature, the reaction mixture was filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography (eluent, ether:hexanes (1:19)) to afford 8 g (62%) of a white solid. m.p. 98-101° C.; 1H NMR (200 MHz, CDCl3) δ 1.41 (6H, d, J=7.2 Hz), 2.38 (3H, s), 3.59 (1H, m), 4.47 (2H, s), 6.86 (1H, s), 6.97 (1H, s), 7.13 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106064B2
Source datasetuspto-grants-2012_01
ORD IDord-726e6e4fd00c4b62a277228d14ad4316
Source noteuspto-grants-2012_01