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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534681Generated: October 31, 2026

Aluminum isopropoxide → HCID 68285922, compound

https://huagongshe.com/reaction/534681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum isopropoxideHCID 11143—
ReactantHCID 68285998HCID 68285998—
SolventIsopropanolHCID 3776—
ProductHCID 68285922HCID 6828592285%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853449B2
Source datasetuspto-grants-2014_10
ORD IDord-a62f435d25514885b0c2bbf9876c0d05
Source noteuspto-grants-2014_10