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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393709Generated: October 25, 2026

Methanol → Sertraline

https://huagongshe.com/reaction/1393709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-(4-(3,4-Dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene)methanamineHCID 9796475—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductSertralineHCID 686170.86%

Reaction Steps

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 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° C. 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 to 89/9 to 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%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345201B2
Source datasetuspto-grants-2008_03
ORD IDord-bd0fab72ac45493e833e6690a8976ecb
Source noteuspto-grants-2008_03