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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1979282Erstellt: 25. Oktober 2026

Sodium Azide → 5-(S)-Azidomethyloxazolidine-2-one

https://huagongshe.com/reaction/1979282

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium AzideHCID 33557—
Edukt1-Butanaminium, N,N,N-tributyl-, azideHCID 5743232—
Edukt(5R)-5-(chloromethyl)-1,3-oxazolidin-2-oneHCID 7058041—
LösungsmittelAcetoneHCID 180—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-(S)-Azidomethyloxazolidine-2-oneHCID 22977318—

Reaktionsschritte

5-(R)-Chloromethyloxazolidine-2-one (prepared according to [Danielmeier et al. Efficient Pathways to (R)- and (S)-hydroxymethyl-2-oxazolidinone and some derivatives. Tetrahedron: Asymmetry. 1995, vol. 6, pp. 1181-1190] (5 mmol) is reacted with sodium azide (7-10 mmol) in acetone (ca. 40-50 mL) at r.t. for ca. 24 h (until the reaction is completed). Solids are filtered off, and supernatant evaporated under vacuum to afford the product which is immediately used for the next step. Optionally, the synthesis is performed in dry N,N-dimethylformamide under inert atmosphere with sodium azide (5-10 mmol) or tetrabutylammonium azide (5-10 mmol), and the resulting solution of the crude 5-(S)-azidomethyloxazolidine-2-one is employed for the next step without solvent removal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06239152B1
Quelldatensatzuspto-grants-2001_05
ORD IDord-59df81ced1b04f56b198111e95c396a4
Quellennotizuspto-grants-2001_05