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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248916Generated: November 1, 2026

Bromide ion → Perbenzoic acid

https://huagongshe.com/reaction/2248916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantHydrogen PeroxideHCID 784—
ReactantDiethyl EtherHCID 3283—
ReactantChloroselenobenzeneHCID 21928—
ReactantBenzenesulfinyl chlorideHCID 4190003—
SolventDichloromethaneHCID 6344—
ProductPerbenzoic acidHCID 523077—

Reaction Conditions

Temperature0 °C

Reaction Steps

The diene (2) is treated with a halogenating agent such as phenylselenyl chloride or bromide or phenylsulfinyl chloride, preferably phenylselenyl chloride, in an approximately equimolar ratio in an inert solvent at about -80° C, for approximately 20 minutes; illustrative of such inert solvents are methylene chloride, ether and the like. After a standard workup the product residue is dissolved in an ethereal solvent, chilled to about 0° C. and oxidized with an agent such as 30% hydrogen peroxide or a peroxy acid such as peroxybenzoic acid to yield a haloghydrin analog (3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041562
Source datasetuspto-grants-1991_08
ORD IDord-4aac0920aa574e8985f12e156f03ca20
Source noteuspto-grants-1991_08