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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065464Generated: October 31, 2026

Bromobenzene → (S)-1-Phenylpiperidine-3-carboxylic acid

https://huagongshe.com/reaction/2065464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
Reactant1,4-DioxaneHCID 31275—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantSodium t-butoxideHCID 23676156—
Reactant(3S)-piperidine-3-carboxylic acid hydrochlorideHCID 24820453—
Catalystpalladium(II) acetateHCID 167845—
Product(S)-1-Phenylpiperidine-3-carboxylic acidHCID 66743624—

Reaction Steps

A mixture of bromobenzene (0.82 mL, 0.0078 mol), (3S)-piperidine-3-carboxylic acid hydrochloride (6.5 mmol, 0.0065 mol), sodium tert-butoxide (1.2 g, 0.013 mol), palladium acetate (40 mg, 0.0002 mol) and 2-(di-tert-butylphosphino)biphenyl (60 mg, 0.0002 mol) was degassed under vacuum and charged with nitrogen. To the mixture was added 1,4-dioxane (20 mL, 0.2 mol) and the resulting mixture was refluxed overnight. After cooling the reaction mixture to ambient temperature, the mixture was filtered and the filtrate was adjusted with TFA to pH=3.0 and extracted with EtOAc. The crude product was used in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288417B2
Source datasetuspto-grants-2012_10
ORD IDord-2a2993ec58964d6b85f7f70072e87556
Source noteuspto-grants-2012_10