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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187901Generated: October 30, 2026

Piperidine → HCID 68881866, compound

https://huagongshe.com/reaction/2187901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3-BromobenzaldehydeHCID 76583—
Reactant4-Mesylphenylacetic acidHCID 572345—
SolventTolueneHCID 1140—
ProductHCID 68881866HCID 68881866—

Reaction Steps

Aryl Bromide AB1 was prepared by the following procedure. To a solution of 3-bromobenzaldehyde (12.9 g, 70 mmol) in toluene (100 mL) was added 4-(methylsulfonyl)phenylacetic acid (15 g, 70 mmol) and piperidine (2 mL). After overnight refluxing, the mixture was cooled down to r.t. To the slurry thus formed, toluene was added (10 mL). Filtration gave (E)-3-(3-Bromophenyl)-2-[4-(methylsulfonyl)phenyl]-2-propenoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410563B1
Source datasetuspto-grants-2002_06
ORD IDord-f9de0470266c4cc283b591fd3d5b5f74
Source noteuspto-grants-2002_06