HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1038831Erstellt: 26. Oktober 2026
L-Methionine → Benzyl 4-cyano-4-methylpiperidine-1-carboxylate
https://huagongshe.com/reaction/1038831
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | L-Methionine | HCID 6137 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Edukt | Benzyl 4-cyanopiperidine-1-carboxylate | HCID 22028286 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Benzyl 4-cyano-4-methylpiperidine-1-carboxylate | HCID 66980706 | 80,3% |
Reaktionsschritte
LiHMDS (47.6 mL, 47.6 mmol) was added dropwise via syringe to the mixture of benzyl 4-cyanopiperidine-1-carboxylate (8.00 g, 31.8 mmol, [Oakwood]) in THF (50 mL) at about −78° C. and stirred for about 1 h. Met (6.76 g, 47.6 mmol) was added dropwise via syringe at about −78° C. and the mixture was stirred overnight at rt. The solution was cooled to 0° C. and saturated aqueous NH4Cl (200 mL) was added. The mixture was extracted with DCM (3×300 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The sample was deposited onto silica gel and purified by column chromatography eluting with 10:1 pet ether/EtOAc to give benzyl 4-cyano-4-methylpiperidine-1-carboxylate (6.6 g, 74%): LC/MS (Table 2, Method i) Rt=2.03 min; MS m/z: 259 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08551981B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-636345933a4e4599a0d0118cb39ab536 |
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| Quellennotiz | uspto-grants-2013_10 |
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