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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1906999Erstellt: 27. Oktober 2026

18-Crown-6 → 2-Nitro-2-methyl-1-[di-(t-butyl)methoxy]propane

https://huagongshe.com/reaction/1906999

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt18-Crown-6HCID 28557—
Edukt2-Nitro-1-propeneHCID 78486—
Edukt2,2,4,4-Tetramethylpentan-3-olHCID 139790—
EduktCID 53628100HCID 178418400—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Nitro-2-methyl-1-[di-(t-butyl)methoxy]propaneHCID 20201202—

Reaktionsschritte

Di-t-butylmethanol is added to a dry flask under argon at 0° C. Dry tetrahydrofuran is added with a syringe. Sec-Butyl lithium (1.5M in Hexanes) is added quickly in one portion and the contents of the flask are stirred for one hour at room temperature. A 10 mM solution of 18-crown-6-ether in acetonitrile is added with a syringe and the flask cooled to 0° C. A tetrahydrofuran solution of 2-nitropropene is added with vigorous stirring over a 10 minute period. After completion of the reaction, as judged by thin layer chromatography, it is quenched with dimethyl sulfate, poured into saturated ammonium chloride and extracted with ethyl acetate. The organic layer is dried over MgSO4 and evaporated to yield 2-nitro-2-methyl-1-[di-(t-butyl)methoxy]propane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04654439
Quelldatensatzuspto-grants-1987_03
ORD IDord-a721fd9b46e9420e949ffa01b97e77ca
Quellennotizuspto-grants-1987_03