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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809469Generated: October 30, 2026

Benzoyl Peroxide → HCID 68632004, compound

https://huagongshe.com/reaction/1809469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactantmethyl 3-bromo-5-fluoro-2-methylbenzoateHCID 68633230—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 68632004HCID 68632004—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of (E4), NBS (1.2 eq.) and benzoyl peroxide (0.1 eq.) in CCl4 (0.28 M) was heated to reflux for 4.5 h. Afterwards, the reaction mixture was cooled down to 0° C. and the solid filtered off. The solid was washed with Et2O and the filtrate was washed sequentially with 1 M Na2S2O3, brine and dried (Na2SO4). Evaporation of the solvent under reduced pressure afforded the title compound that was used without further purification in the next step. 1H NMR (400 MHz, CDCl3, 300 K) δ 7.63 (1H, dd, J=8.6 and 2.8 Hz), 7.52 (1H, dd, J=7.4 and 2.8 Hz), 5.10 (2H, s), 3.97 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362030B2
Source datasetuspto-grants-2013_01
ORD IDord-ed7b6d142d744fc8a1e78924a64e69ba
Source noteuspto-grants-2013_01