HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359029Generated: November 3, 2026
4-Methoxybenzenesulfonyl chloride → HCID 53981330, compound
https://huagongshe.com/reaction/1359029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 54437399 | HCID 54437399 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53981330 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599890B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-29e08e24d25e4e16bbb5d8ec3b5c24fb |
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| Source note | uspto-grants-2003_07 |
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