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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390137Generated: October 26, 2026

Piperidine → Tert-butyl(4-chloro-2-{[2-methyl-5-(propylsulfonyl)phenyl]ethynyl}phenoxy)acetate

https://huagongshe.com/reaction/2390137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTert-butyl(4-chloro-2-ethynylphenoxy)acetateHCID 56594381—
Reactant2-Bromo-1-methyl-4-(propylsulfonyl)benzeneHCID 58522091—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl(4-chloro-2-{[2-methyl-5-(propylsulfonyl)phenyl]ethynyl}phenoxy)acetateHCID 58521875—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2-bromo-1-methyl-4-(propylsulfonyl)benzene (Intermediate 37; 14.86 g, 53.6 mmol), tert-butyl(4-chloro-2-ethynylphenoxy)acetate (Intermediate 3, 13.00 g; 48.7 mmol), dichlorobis(triphenylphosphine)palladium(II) (1.37 g; 1.95 mmol) and piperidine (14.5 mL) was heated at 70° C. for 18 hours. The reaction mixture was taken up in EtOAc, washed twice with ammonium chloride and once with brine. The organic phase was dried over MgSO4, filtered and concentrated to dryness affording a crude, which was purified by flash column chromatography (silica), eluting with cyclohexane containing increasing amounts of EtOAc. The compound thus obtained as a brown sticky solid was recrystallized twice from EtOAc/petroleum ether to afford the title compound as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273769B2
Source datasetuspto-grants-2012_09
ORD IDord-27458ffdb07e4658b50be3bec3f780e0
Source noteuspto-grants-2012_09