Phosphinic Acid → Bis(3,4-dimethoxyphenyl)ditelluride

HRID 2352053Notes

Reaction equation

HRID 2352053 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([Te:11](Cl)(Cl)Cl)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[PH2](O)=O>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([Te:11][Te:11][C:5]2[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]

Participants

4

Reactant 2

HCID 4124402Phosphinic AcidHCID 124943393,4-Dimethoxyphenyltellurium trichloride

Product 1

HCID 4345922Bis(3,4-dimethoxyphenyl)ditelluride

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

3,4-Dimethoxyphenyltellurium trichloride (37.2 g=0.1 mole) was dissolved in absolute ethanol (500 ml), and the slightly turbid solution was filtered. To the rapidly stirred solution was added, at room temperature, 50% aqueous hypophosphorous acid (30 ml, ≃0.3 mole) as rapidly as possible. There was a brief appearance of a brown solution color, before the entire solution set to a mass of black fibrous crystals. The product was collected after 15 minutes by filtration using rubber dam to compact the highly solvated crystal mass. The product was washed with water and then air dried to yield 25.2 g, 95% of theory, black fibrous crystals, m.p. 134°-136° C. Recrystallization from isopropanol raised the m.p. to 136°-139° C. C, H and Te elemental analyses were in agreement with the structural formula.

Workup

  1. filtrationthe slightly turbid solution was filtered
  2. additionTo the rapidly stirred solution was added, at room temperature
  3. filtrationThe product was collected after 15 minutes by filtration
  4. washThe product was washed with water
  5. customair dried
  6. customto yield 25.2 g, 95% of theory, black fibrous crystals, m.p. 134°-136° C
  7. customRecrystallization from isopropanol
  8. temperatureraised the m.p. to 136°-139° C

Sources & evidence

ORD record
ord-e043621f414a48caa772227eed0e3acd
Source dataset
uspto-grants-1989_10
Patent number
US04874866

Reaction notes

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