Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1007661Erstellt: 24. Oktober 2026

Anisole → Methanone, (2-chlorophenyl)phenyl-

https://huagongshe.com/de/reaction/1007661

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnisoleHCID 7519—
EduktBenzoyl chloride, 2-chloro-5-nitro-HCID 117637—
EduktAluminum(III) ChlorideHCID 6451240—
ProduktMethanone, (2-chlorophenyl)phenyl-HCID 78838—

Reaktionsschritte

Compound 29 was prepared by reacting 2-chloro-5-nitrobenzoic acid chloride with anisole in the presence of aluminum trichloride to produce a chlorobenzophenone compound; the chlorobenzophenone compound was reduced in the presence of trifluoromethanesulfonic acid and triethylsilane to produce a chlorodiphenylmethane compound; the chlorodiphenylmethane compound was treated with lithium sulfide and 2,2-dibutyl-3-(methanesulfonato)propanal to produce 1-(2,2-dibutyl-3-oxopropylthio)-2-((4-methoxyphenyl)methyl)-4-dimethylaminobenzene (40); and 40 was oxidized with m-chloroperbenzoic acid to produce 29. The first step of that method of preparing compound 29 requires the use of a corrosive and reactive carboxylic acid chloride that was prepared by the reaction of the corresponding carboxylic acid with phosphorus pentachloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06794544B2
Quelldatensatzuspto-grants-2004_09
ORD IDord-ea99c8a26ce44f1aae383e2d7327620f
Quellennotizuspto-grants-2004_09