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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460659Generated: October 26, 2026

4-(4-Chloro-3-fluorophenyl)piperidine → (S)-alpha-(2'-(3-(4-(4-chloro-3-fluorophenyl)piperidino)-2-hydroxypropyloxy)benzylidene)-gamma-butyrolactone

https://huagongshe.com/reaction/460659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chloro-3-fluorophenyl)piperidineHCID 16679313—
Reactant(S)-alpha-(2'-(2,3-epoxypropan-1-yloxy)benzylidene)-gamma-butyrolactoneHCID 86585643—
SolventMethanolHCID 887—
Product(S)-alpha-(2'-(3-(4-(4-chloro-3-fluorophenyl)piperidino)-2-hydroxypropyloxy)benzylidene)-gamma-butyrolactoneHCID 6990148833.7%

Reaction Steps

By the reaction 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-fluorophenyl)piperidine (0.8 g) in methanol (50 ml), the title compound (0.58 g), melting point 114–115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196199B2
Source datasetuspto-grants-2007_03
ORD IDord-319df2f82449400299a54d47a1c90779
Source noteuspto-grants-2007_03