Reaktion #215247

ord-586e5e10a57d46a2ac260a0067ccd962

Reaktionsgleichung

CC(=O)OCCOC(C)=O
ethylene glycol diacetate
BrCC[Te](Br)(Br)CCBr
bis(2-bromoethyl)-tellurium dibromide
OCCO
ethylene glycol
CC(=O)OCCBr
2-bromoethylacetate
O=O
oxygen
BrCC[Te](Br)(Br)CCBr
bis(2-bromoethyl)tellurium dibromide
C=C
ethylene
BrCCBr
ethylene dibromide
CC(=O)OCCOC(C)=O
ethylene glycol diacetate
CC(=O)OCCBr
2-bromoethylacetate
CC(Br)Br
dibromoethane

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeglass tube reactor equipped with a gas inlet and outlet tube
  2. 2
    TemperaturThe reaction mixture was cooled
  3. 3
    Sonstigepartition chromagraph (glpc.)

Vorschrift

1.05 g. (2.09 mmoles) of bis(2-bromoethyl)-tellurium dibromide, from Example 2, along with 4.0 g. glacial acetic acid (99.5 percent) was charged to a "Fisher-Porter" 35 ml. glass tube reactor equipped with a gas inlet and outlet tube, a pressure gauge and relief valve and a magnetic stirrer. The mixture was heated at a temperature of 150° C. under 16 psig oxygen with stirring for 1 hour. The reaction mixture was cooled and the products analyzed by gas liquid partition chromagraph (glpc.) showed 3.10 mmoles of ethylene glycol diacetate, 0.79 mmoles of 2-bromoethylacetate, 0.12 mmoles ethylene dibromide and a trace amount of ethylene. Based on stoichiometry that one mole of bis(2-bromoethyl)tellurium dibromide yields two moles of ethylene glycol precursors, i.e., ethylene glycol diacetate, 2-bromoethylacetate and dibromoethane, the mass balance was calculated to be 96 mole percent.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04258208uspto-grants-1981_03