HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534681Generated: October 31, 2026
Aluminum isopropoxide → HCID 68285922, compound
https://huagongshe.com/reaction/534681
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminum isopropoxide | HCID 11143 | — |
| Reactant | HCID 68285998 | HCID 68285998 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 68285922 | HCID 68285922 | 85% |
Reaction Steps
Aluminium isopropoxide (2.05 g, 10.0 mmol) is added to a solution of the compound obtained in Step B (680 mg, 3.15 mmol) in isopropanol (15 mL) at ambient temperature. The reaction mixture is refluxed. When the reagents have been completely consumed, a few crystals of p-toluenesulphonic acid monohydrate are added and a Dean-Stark apparatus is mounted on top of the flask. The mixture is again refluxed for 1 hour, during which the isopropanol is gradually replaced with toluene by means of the Dean-Stark apparatus. A 1N HCl solution is then added and the resulting phases are separated. The aqueous phase is extracted with ethyl acetate, the organic phases being washed with saturated NaHCO3 solution and with saturated NaCl solution, then dried over MgSO4, filtered and concentrated under reduced pressure. The residue is purified by column chromatography (petroleum ether-ethyl acetate: 80-20) to yield the title product in the form of an oil in a yield of 85%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853449B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-a62f435d25514885b0c2bbf9876c0d05 |
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| Source note | uspto-grants-2014_10 |
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