HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 712207Erstellt: 24. Oktober 2026
Hexane → 1-tert-Butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate
https://huagongshe.com/de/reaction/712207
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hexane | HCID 8058 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | Tert-butyl 4-cyanopiperidine-1-carboxylate | HCID 1514443 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-tert-Butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate | HCID 57750376 | 48% |
Reaktionsschritte
A solution of tert-butyl 4-cyanopiperidine-1-carboxylate (0.75 g, 3.57 mmol) in THF (25.0 mL) was cooled to −78° C. followed by dropwise addition of LDA (1.8 M in THF, 6.0 mL, 5.35 mmol) and stirred at the same temperature (−78° C.) for 45 min followed by addition of ethyl chloroformate (0.46 g, 4.28 mmol). The temperature of the reaction was slowly raised to rt and left to stir for 6 h. The reaction was then cooled to 0° C. and quenched by drop wise addition of saturated NH4Cl solution (50 mL), extracted with EtOAc (3×100 mL) and the combined organics washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure. The crude residue was purified over 100-200 M silica-gel using 7% EtOAc:hexane to obtain the product as an orange viscous liquid (0.4 g, 48% yield). MS: 283.14 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09181234B2 |
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| Quelldatensatz | uspto-grants-2015_11 |
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| ORD ID | ord-09798f3e46594c668a7a06e7d4b56e82 |
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| Quellennotiz | uspto-grants-2015_11 |
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