Réaction #1552044

ord-b899b364a99e4587b4d92ddc37db41c7

Équation de réaction

C=COC(=O)Cl
chloroformic acid vinyl ester
CCOP(OCC)OCC
triethyl phosphite
C=COC(=O)P(=O)(OCC)OCC
title compound
C=COC(=O)P(=O)(OCC)OCC
vinyloxycarbonyl phosphonic acid diethyl ester

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONAfter completion of the addition
  2. 2
    workup.STIRRINGthe reaction mixture was stirred for further 2 hours at room temperature
  3. 3
    AutreFor complete removal of the ethyl chloride
  4. 4
    Autreformed during the reaction
  5. 5
    Températurethe solution was heated to 40° C. for 30 minutes
  6. 6
    AutrePurification by vacuum destillation

Mode opératoire

2.0 g (19 mmol) of chloroformic acid vinyl ester were precharged into a 50 ml two-necked flask, and, while stirring at 0° C., 3.13 g (19 mmol) of triethyl phosphite were slowly added dropwise. After completion of the addition, the reaction mixture was stirred for further 2 hours at room temperature. For complete removal of the ethyl chloride formed during the reaction, the solution was heated to 40° C. for 30 minutes. Purification by vacuum destillation yielded 2.5 g (64% of th.) of the title compound as a colorless liquid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08999323B2uspto-grants-2015_04