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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1015721Erstellt: 24. Oktober 2026

Hydrochloric Acid → 3-Chloro-5-(methylthio)benzonitrile

https://huagongshe.com/de/reaction/1015721

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDiisopropylethylamineHCID 81531—
EduktSodium methanethiolateHCID 4378561—
Edukt3-Bromo-5-chlorobenzonitrileHCID 15965893—
Katalysator1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
Produkt3-Chloro-5-(methylthio)benzonitrileHCID 6687868676,6%

Reaktionsschritte

(Step 1) A mixture of 3-bromo-5-chlorobenzonitrile (4.0 g), sodium methanethiolate (1.42 g), Pd2(dba)3 (84 mg), Xantphos (106 mg) and N,N-diisopropylethylamine (4.78 g) was stirred in toluene (100 ml) at 90° C. for 9 hr. The reaction mixture was treated with 1N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:20) to give 3-chloro-5-(methylsulfanyl)benzonitrile (2.6 g) as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07985862B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-61f2e09ff6c84555838fd9b8e48fb3a8
Quellennotizuspto-grants-2011_07