Benzene → Yttrium(iii) isopropoxide

HRID 2164712Notes

Reaction equation

HRID 2164712 reaction equation
[CH3:1][CH:2]([CH3:4])[O-:3].[Li+].[CH:6]([OH:9])([CH3:8])[CH3:7].[Cl-].[Cl-].[Cl-].[Y+3:13].C1C=CC=CC=1>O1CCCC1>[CH3:1][CH:2]([CH3:4])[O-:3].[Y+3:13].[CH3:7][CH:6]([CH3:8])[O-:9].[CH3:1][CH:2]([CH3:4])[O-:3]

Participants

6

Procedure

Lithium isopropoxide (24.3 g, 0.37 mol.) and isopropyl alcohol (150 ml) were placed in a round-bottomed flask of a 300 ml-capacity, to which was then added dropwise a solution of anhydrous yttrium trichloride (23.4 g, 0.12 mol.) in 25 ml of tetrahydrofuran under stirring. After the addition of the yttrium trichloride, the mixture in the flask was stirred at 45° C. for 3 hours with heating by means of a mantle heater, followed by concentration of the reaction solution to dryness by evaporation of the solvent. The residue obtained was admixed with 150 ml of benzene and the resultant solution was filtered to remove the insoluble matter. Distillation off of the benzene from the filtered solution gave 16.8 g of yttrium isopropoxide as a slightly yellow crystal. Yield 52.6%

Workup

  1. stirringthe mixture in the flask was stirred at 45° C. for 3 hours
  2. temperaturewith heating by means of a mantle heater
  3. customfollowed by concentration of the reaction solution to dryness by evaporation of the solvent
  4. customThe residue obtained
  5. filtrationthe resultant solution was filtered
  6. customto remove the insoluble matter
  7. distillationDistillation off of the benzene from the filtered solution

Sources & evidence

ORD record
ord-aaa59bc9b013495e96441fd3f0775609
Source dataset
uspto-grants-1985_03
Patent number
US04507245

Reaction notes

Loading…