HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
18-Crown-6 → 2-Nitro 1-[di-(t-butyl)methoxy]propane
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 18-Crown-6 | HCID 28557 | — |
| Edukt | 2-Nitro-1-propene | HCID 78486 | — |
| Edukt | 2,2,4,4-Tetramethylpentan-3-ol | HCID 139790 | — |
| Edukt | CID 53628100 | HCID 178418400 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Nitro 1-[di-(t-butyl)methoxy]propane | HCID 13907245 | — |
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 saturated ammonium chloride and extracted with ethyl acetate. The organic layer is dried over MgSO4 and evaporated to yield 2-nitro 1-[di-(t-butyl)methoxy]propane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04666729 |
| Quelldatensatz | uspto-grants-1987_05 |
| ORD ID | ord-ecdfd4451c604b1c96a376877cf618d1 |
| Quellennotiz | uspto-grants-1987_05 |