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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1393710Erstellt: 25. Oktober 2026

Methanol → Sertraline

https://huagongshe.com/reaction/1393710

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktN-(4-(3,4-Dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene)methanamineHCID 9796475—
EduktHCID 178418361HCID 178418361—
KatalysatorNickelHCID 935—
LösungsmittelChlorobenzeneHCID 7964—
ProduktSertralineHCID 686170,86%

Reaktionsschritte

N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)naphthalenylidene]methanamine (Ketimine) (50 g), methanol (300 ml), Raney Nickel (0.15 g wet basis) and chlorobenzene (25 ml) are charged into a reaction vessel. The mixture is hydrogenated at 5 to 6 kg/cm2 over pressure of hydrogen for 6 to 7 hrs at about 28 to 30° C. The catalyst is removed by filtration and the cake is washed with 50 ml methanol. The cis to trans ratio is 87-89/9-13. The amount of dehalogenated by product is <0.1%. Sertraline racemate free base thus formed is treated with hydrochloric acid (24 ml, 33%) and predominantly isomer of sertraline HCl racemate is filtered [Cis>98%, trans<2%, dehalogenation product<0.1%, yield 0.86 to 0.88%].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07345201B2
Quelldatensatzuspto-grants-2008_03
ORD IDord-bbf3cdd8ae9b4a6092673f4ae80371ff
Quellennotizuspto-grants-2008_03