HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17864Erstellt: 23. Oktober 2026
Nipecotic Acid → 1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acid
https://huagongshe.com/de/reaction/17864
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Nipecotic Acid | HCID 4498 | — |
| Edukt | Benzyl chloroformate | HCID 10387 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acid | HCID 234339 | — |
Reaktionsschritte
To an ice cooled solution of nipecotic acid (10.0 g, 77.5 mmol), sodium hydroxide (3.4 g, 85 mmol), and tetrahydrofuran (50 mL) in water (100 mL) was added by simultaneous dropwise addition benzylchloroformate (13.3 mL, 93 mmol) in tetrahydrofuran (50 mL) and sodium hydroxide (3.4 g, 85 mmol) in water (50 mL). Warmed slowly to room temperature. After 24 hours tetrahydrofuran was removed in vacuo and the resulting aqueous mixture acidified with 3 N hydrochloric acid and extracted with dichloromethane (3×). The combined organic portions were dried with anhydrous magnesium sulfate. Filtration followed by evaporation of the filtrate in vacuo gave the titled compound. 1HNMR (CHCl3, 300 MHz) □ 7.45-7.20 (m, 5H); 5.14 (m, 2H); 4.21 (br s, 1H); 3.96 (m, 1H), 3.15 (br s, 1H); 2.93 (m, 1H); 2.51 (m, 1H); 2.09 (m, 1H); 1.80-1.60 (m, 2H); 1.50 (m, 1H) ppm.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741322B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-41a63700f6cc44a0b5ecf557890effc5 |
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| Quellennotiz | uspto-grants-2010_06 |
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