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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111034Generated: November 1, 2026

Ethanol → Sertraline

https://huagongshe.com/reaction/2111034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantN-(4-(3,4-Dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene)methanamineHCID 9796475—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductSertralineHCID 686170.8%

Reaction Steps

N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H) naphthalenylidene]methanamine (Ketimine) (50 g), ethanol (300 ml), Raney Nickel (0.15 g wet basis) and o-dichlorobenzene (50 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 ethanol. The cis to trans ratio is 82 to 85/18 to 15. 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 0.80 to 0.82%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07518018B2
Source datasetuspto-grants-2009_04
ORD IDord-b44f11472228454b947d42e9f15f71f3
Source noteuspto-grants-2009_04