Reacción #1552045

ord-49b225158520463ba7cc853d61458f6c

Ecuación de reacción

NC(=O)OC=CO
2-hydroxyvinyl carbamate
C1CCOC1
THF
CCN(CC)CC
triethylamine
CCOP(Cl)OCC
diethylchlorophosphonite
C1CCOC1
THF
C=CNC(=O)O.CCOP(=O)(OCC)OCCN
title compound
C=CNC(=O)O.CCOP(=O)(OCC)OCCN
2-(diethoxyphosphoryloxy)ethylamine vinyl carbamate

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONAfter completion of the addition
  2. 2
    FiltraciónA white solid was filtered off
  3. 3
    Lavadothe residue was washed with a 5% aqueous solution of sodium hydrogen carbonate (3×10 ml)
  4. 4
    SecadoThe organic phase was then dried over sodium sulfate
  5. 5
    FiltraciónAfter filtering off the siccative, the solvent
  6. 6
    Otrowas removed on a rotary evaporator
  7. 7
    OtroThe crude product was purified by column chromatography on silica gel (PE:EE=1:5)

Procedimiento

0.81 ml of triethylamine (5.8 mmol) were precharged in 10 ml of abs. THF, and 0.76 g of 2-hydroxyvinyl carbamate (5.8 mmol) were added. The reaction solution was then cooled to −78° C., and 0.83 ml of diethylchlorophosphonite (5.8 mmol) in 4 ml of THF were added dropwise. After completion of the addition, the reaction mixture was stirred for 12 hours at room temperature. A white solid was filtered off, and the residue was washed with a 5% aqueous solution of sodium hydrogen carbonate (3×10 ml). The organic phase was then dried over sodium sulfate. After filtering off the siccative, the solvent was removed on a rotary evaporator. The crude product was purified by column chromatography on silica gel (PE:EE=1:5). 0.39 g (25% of th.) of the title compound were obtained as a colorless oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08999323B2uspto-grants-2015_04