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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1388536Erstellt: 27. Oktober 2026

Ammonium Chloride → alpha-(-Methyl-4-piperidyl)-2-(2,5-difluorophenylthio)-5-chlorobenzyl alcohol

https://huagongshe.com/reaction/1388536

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt4-chloro-N-methylpiperidineHCID 79342—
EduktMagnesiumHCID 5462224—
Edukt2-(2,5-Difluorophenylthio)-5-chlorobenzaldehydeHCID 12815951—
LösungsmittelTetrahydrofuranHCID 8028—
Produktalpha-(-Methyl-4-piperidyl)-2-(2,5-difluorophenylthio)-5-chlorobenzyl alcoholHCID 12815956100%

Reaktionsschritte

A solution of a Grignard reagent is prepared by reaction of 11.35 g of 4-chloro-1-methylpiperidine with 2.3 g of magnesium in 70 ml of tetrahydrofuran and is then treated for 10 minutes with a solution of 16.1 g 2-(2,5-difluorophenylthio)-5-chlorobenzaldehyde in 40 ml of tetrahydrofuran, added dropwise. The mixture is refluxed for 4 hours and, after cooling, decomposed with a 20% ammonium chloride solution and extracted with benzene. The extract is washed with water, dried with potassium carbonate and evaporated. There are obtained 21.7 g (100%) crude oily α-(-methyl-4-piperidyl)-2-(2,5-difluorophenylthio)-5-chlorobenzyl alcohol which is used in this state for the final step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04431808
Quelldatensatzuspto-grants-1984_02
ORD IDord-d345d77a6ad94402b481c2e7ad6d78e7
Quellennotizuspto-grants-1984_02