Reaktion #352775

ord-1f4786ecea854207ac7614b77f66a780

Reaktionsgleichung

C=CC(=O)OCCO
2-Hydroxyethyl acrylate
CCN(CC)CC
triethylamine
O=P1(Cl)OCCO1
2-chloro-2-oxo-1,3,2-dioxaphospholane
C=CC(=O)OCCOP1(=O)OCCO1
oil
C=CC(=O)OCCOP1(=O)OCCO1
2-(2-Oxo-1,3,2-dioxaphospholan-2-yloxy)ethyl acrylate

Reaktionsbedingungen

Temperatur
-20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added over 20 minutes
  2. 2
    Temperaturto warm to 10° C. over a further hour
  3. 3
    FiltrationThe precipitate was filtered
  4. 4
    Waschenwashed with ethyl acetate (100 ml)
  5. 5
    Sonstigethe combined filtrate and washings evaporated under reduced pressure

Vorschrift

2-Hydroxyethyl acrylate (11.5 ml, 0.1M) and triethylamine (14.6 ml) in dry diethyl ether (250 ml) were cooled to -25° C. under nitrogen as a solution of 2-chloro-2-oxo-1,3,2-dioxaphospholane (14.3 g) in dry diethyl ether was added over 20 minutes. The mixture was stirred for a further 1 hour at -20° C. and then allowed to warm to 10° C. over a further hour. The precipitate was filtered, washed with ethyl acetate (100 ml) and the combined filtrate and washings evaporated under reduced pressure to give a pale yellow oil (21 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05648442uspto-grants-1997_07