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HRID 1979282생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1979282

반응식

참여 물질

역할이름HCID투입량
반응물Sodium AzideHCID 33557—
반응물1-Butanaminium, N,N,N-tributyl-, azideHCID 5743232—
반응물(5R)-5-(chloromethyl)-1,3-oxazolidin-2-oneHCID 7058041—
용매AcetoneHCID 180—
용매DimethylformamideHCID 6228—
생성물5-(S)-Azidomethyloxazolidine-2-oneHCID 22977318—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06239152B1
출처 데이터셋uspto-grants-2001_05
ORD IDord-59df81ced1b04f56b198111e95c396a4
출처 메모uspto-grants-2001_05