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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460660Generated: October 29, 2026

4-[4-Chloro-3-(trifluoromethyl)phenyl]piperidine → (S)-alpha-(2'-(3-(4-(4-chloro-3-trifluoromethylphenyl)piperidino)-2-hydroxypropyloxy) benzylidene)-gamma-butyrolactone Hydrochloride Monohydrate

https://huagongshe.com/reaction/460660

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[4-Chloro-3-(trifluoromethyl)phenyl]piperidineHCID 16679317—
ReactantHydrochloride methanolHCID 21893726—
Reactant(S)-alpha-(2'-(2,3-epoxypropan-1-yloxy)benzylidene)-gamma-butyrolactoneHCID 86585643—
SolventMethanolHCID 887—
Product(S)-alpha-(2'-(3-(4-(4-chloro-3-trifluoromethylphenyl)piperidino)-2-hydroxypropyloxy) benzylidene)-gamma-butyrolactone Hydrochloride MonohydrateHCID 6949779152.6%

Reaction Steps

The reaction was performed in same manner as in Example 307 using (S)-α-(2′-(2,3-epoxypropan-1-yloxy)benzylidene)-γ-butyrolactone (1.0 g) and 4-(4-chloro-3-trifluoromethylphenyl)piperidine (0.8 g) in methanol (50 ml), and the obtained oil was treated with methanol/hydrochloric acid to give the title compound (0.45 g), melting point 172–174° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196199B2
Source datasetuspto-grants-2007_03
ORD IDord-f0ef088f4f2049c3943f949991cc5401
Source noteuspto-grants-2007_03