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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583124Generated: November 1, 2026

Piperidine → HCID 68881866, compound

https://huagongshe.com/reaction/1583124

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 numberUS06740666B2
Source datasetuspto-grants-2004_05
ORD IDord-1c0d5b44b439496c9b179c1f3a7f3d4c
Source noteuspto-grants-2004_05