Reaction #1563877

ord-1ef80601a31a4f4da61e86fe27df8d55

Reaction equation

O=C(c1ccco1)C1Oc2c(Cl)c(Cl)c(Cl)c(Cl)c2O1
furan-2-yl(4,5,6,7-tetrachlorobenzo[d][1,3]dioxol-2-yl)methanone
NNc1ccccc1
phenylhydrazine
C(=NNc1ccccc1)/C(=N\Nc1ccccc1)c1ccco1
(2E)-2,2′-(1-(furan-2-yl)ethane-1,2-diylidene)bis(1-phenylhydrazine)
Yield 87.0%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperaturewas heated
  2. 2
    Temperatureunder reflux for 30 minutes
  3. 3
    OtherDuring the course of the reflux, a yellow solid initially precipitated
  4. 4
    workup.DISSOLUTIONdissolved upon further heating
  5. 5
    OtherThe solvent was evaporated to dryness

Procedure

A mixture of furan-2-yl(4,5,6,7-tetrachlorobenzo[d][1,3]dioxol-2-yl)methanone (200 mg, 0.568 mmol) and phenylhydrazine (185 mg, 1.704 mmol) in ethanol (3 ml) was heated under reflux for 30 minutes. During the course of the reflux, a yellow solid initially precipitated, but then dissolved upon further heating. The solvent was evaporated to dryness, and the resulting crude material was subjected to flash column chromatography using 7% ethyl acetate/hexane as an eluent to yield (2E)-2,2′-(1-(furan-2-yl)ethane-1,2-diylidene)bis(1-phenylhydrazine) as a yellow solid (150 mg, 87%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09402397B2uspto-grants-2016_08