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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 330094Erstellt: 24. Oktober 2026

Bromide ion → Perbenzoic acid

https://huagongshe.com/de/reaction/330094

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromide ionHCID 259—
EduktHydrogen PeroxideHCID 784—
EduktDiethyl EtherHCID 3283—
EduktChloroselenobenzeneHCID 21928—
EduktBenzenesulfinyl chlorideHCID 4190003—
LösungsmittelDichloromethaneHCID 6344—
ProduktPerbenzoic acidHCID 523077—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

In a general description of scheme 1 the diene (2) of step (A) 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 halohydrin analog (1-3).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04894465
Quelldatensatzuspto-grants-1990_01
ORD IDord-206018e1ceb74cfdb888d82f842d23c3
Quellennotizuspto-grants-1990_01