Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1479149Erstellt: 25. Oktober 2026

Water → tert-butyl N-ethenylcarbamate

https://huagongshe.com/reaction/1479149

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium HydroxideHCID 14798—
Edukttert-Butyl methyl etherHCID 15413—
Edukttert-butyl N-ethenyl-N-formylcarbamateHCID 89760727—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-butyl N-ethenylcarbamateHCID 251740—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

A solution of N-formyl-N-vinyl-carbamic acid tert-butyl ester (103.6 g, crude 89% pure, 539 mmol) in THF (320 ml) was cooled to 0° C. and stirred rapidly. NaOH (2M, 323 ml, 6.46 mmol) was slowly added over ca 20 minutes. The internal temperature rose to 19° C., and began then to cool. After cooling to 5° C. the mixture was warmed to RT. After 1 hour the reaction was finished according to tlc and GC. The reaction mixture was shaken between tBuOMe (250 ml) and water (250 ml), washed with water (250 ml) and brine (250 ml), dried over MgSO4 and evaporated. The product was a yellow oil containing traces of THF (NMR). The crude product was dissolved in pentane (25 ml), seeded, and left overnight at −20° C. The colourless crystals were swirled in pentane, filtered off and washed 3× with pentane, then spread in the air to dry to yield 48.9 g (63%). The mother liquors were evaporated down, dissolved in a little pentane and seeded. A further 8.1 g (11%) was isolated. (The product can also be sublimed/distilled.) m.p. 67-68° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09408392B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-8868d29f29de46fb945c49b5a275b9c2
Quellennotizuspto-grants-2016_08