Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Yttrium trichloride | HCID 10198055 | — |
| Reactant | Lithium propan-2-olate | HCID 23673350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Yttrium(iii) isopropoxide | HCID 11550724 | 52.6% |
Reaction Steps
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%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04507245 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-aaa59bc9b013495e96441fd3f0775609 |
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| Source note | uspto-grants-1985_03 |
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