HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 408578Erstellt: 26. Oktober 2026
Acetic Acid → 1-Benzyl-2-methyl-azetidine-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/408578
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Edukt | 2-[Benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl ester | HCID 70557779 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-Benzyl-2-methyl-azetidine-2-carboxylic acid ethyl ester | HCID 70558658 | — |
Reaktionsschritte
A solution of 2-[benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl ester (1 eq.) in dry THF was cooled to −78° C. under nitrogen. KHMDS (15% w/w in toluene) (1.25 eq.) was slowly added so that temperature was kept below −65° C. The reaction was stirred for 1 h at −70° C. Then acetic acid (0.3 eq.) was added. The reaction was warmed to 20° C. and stirred for 10 min, then quenched with a saturated aqueous solution of NaHCO3 and partially concentrated under reduced pressure. The crude was extracted twice with DCM. The organic layers were combined, dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc 1/0 then 95/5) to afford 1-benzyl-2-methyl-azetidine-2-carboxylic acid ethyl ester.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08759334B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-f490badee2424203bebb3fd33a4da7a0 |
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| Quellennotiz | uspto-grants-2014_06 |
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