HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 397663Erstellt: 25. Oktober 2026
4-Fluorobenzenesulfonyl chloride → (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylic acid
https://huagongshe.com/reaction/397663
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Edukt | N,N-Diethyl-2-propanamine | HCID 521913 | — |
| Edukt | (2S)-2-Piperidinecarboxylic acid L-tartrate | HCID 69946027 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Sodium Hydroxide | HCID 14798 | — |
| Produkt | (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylic acid | HCID 768662 | 96,1% |
Reaktionsschritte
(2S)-2-Piperidinecarboxylic acid L-tartrate (10 g) [see Preparation 1] was dissolved in 1N aqueous sodium hydroxide solution (107.4 ml) and diethylisopropylamine (9.35 ml) was added followed by a solution of 4-fluorobenzenesulphonyl chloride (10.45 g) in acetone (107 ml) at 0° C. The reaction mixture was warmed to room temperature and stirred for 18 hours after which time the solvent was removed under reduced pressure and the residue diluted with 1N aqueous sodium hydroxide solution. The aqueous solution was washed with diethyl ether and acidified with concentrated hydrochloric acid. The product was extracted with ethyl acetate, the organic layers dried over magnesium sulphate and the solvent was removed under reduced pressure to afford (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylic acid (9.89 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06610707B1 |
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| Quelldatensatz | uspto-grants-2003_08 |
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| ORD ID | ord-870f1d9bb4b247fbb5b6db8f1ee452a0 |
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| Quellennotiz | uspto-grants-2003_08 |
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