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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359029Generated: November 3, 2026

4-Methoxybenzenesulfonyl chloride → HCID 53981330, compound

https://huagongshe.com/reaction/1359029

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantTriethylamineHCID 8471—
ReactantHCID 54437399HCID 54437399—
SolventDichloromethaneHCID 6344—
ProductHCID 53981330HCID 53981330—

Reaction Steps

To a stirred, cold (0° C.) solution of (2R,4R)-piperidine-2,4-dicarboxylic acid 2-tert-butyl ester 4-methyl ester (2.7 g, 11.1 mmol) and triethylamine (4.6 ml, 33.3 mmol) in 30 mL of methylene chloride was added 4-methoxy-benzenesulfonyl chloride (2.3 g, 11.1 mmol). The mixture was warmed to ambient temperature and stirred for 4 hours. The reaction was quenched by the addition of aqueous ammonium chloride and the mixture was extracted with ethyl acetate. The combined organic extracts were washed with brine, and the organic mixture was dried over sodium sulfate. After filtration and concentration of the filtrate, the resulting crude product was purified by silica gel chromatography (elution with 3:8 ethyl acetate/hexanes) to provide (2R,4R)-1-(4-methoxy-benzenesulfonyl)-piperidine-2,4-dicarboxylic acid 2-tert-butyl ester 4-methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599890B1
Source datasetuspto-grants-2003_07
ORD IDord-29e08e24d25e4e16bbb5d8ec3b5c24fb
Source noteuspto-grants-2003_07