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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867999Generated: October 25, 2026

Sertraline → Sertraline, cis-(-)-

https://huagongshe.com/reaction/867999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSertralineHCID 68617—
Reactant4-(3,4-Dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenoneHCID 3746251—
Reactant4-(3,4-Dichlorophenyl)-4-phenylbutanoic acidHCID 9904723—
ProductSertraline, cis-(-)-HCID 54375—

Reaction Steps

As previously indicated, the 4-(3,4-dichlorophenyl)-4-phenylbutanoic acid final product afforded by the process of this invention is a valuable intermediate that ultimately leads to the antidepressant agent known as sertraline or cis-(1S) (4S)-N-methyl-4-(3,4-dichlorophenyl)-1, 2,3,4-tetrahydro-1-naphthaleneamine as disclosed in the previously discussed prior art. More specifically, 4-(3,4-dichlorophenyl)-4-phenylbutanoic acid is first converted to 4-(3,4-dichlorophenyl)-3, 4-dihydro-1-(2H)-naphthalenone and then finally to racemic cis-N-methyl-4-(3,4-dichlorophenyl)-1, 2,3,4-tetrahydro-1-naphthaleneamine prior to ultimately yielding the desired cis-(1S) (4S)-N-methyl-4-(3,4-dichlorophenyl)-1, 2,3,4-tetrahydro-1-naphthaleneamine by the multi-step method of the prior art process as earlier described by W.M. Welch, Jr. et al. in U.S. Pat. No. 4,536,518 and the Journal of Medicinal Chemistry, Vol. 27, No. 11, p. 1508 (1984).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04777288
Source datasetuspto-grants-1988_10
ORD IDord-99645623274745aa8584a0a30c4cef90
Source noteuspto-grants-1988_10