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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249635Generated: November 2, 2026

Oxalyl chloride → 5-(2,4-Diisobutoxybenzoyl)-2-isobutoxyphenyl acetate

https://huagongshe.com/reaction/2249635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1,3-DiisobutoxybenzeneHCID 13087565—
Reactant3-(Acetyloxy)-4-isobutoxybenzoic acidHCID 17816473—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-(2,4-Diisobutoxybenzoyl)-2-isobutoxyphenyl acetateHCID 1781645768.5%

Reaction Steps

In 10 ml of methylene chloride is dissolved 1.00 g of 3-(acetyloxy)-4-isobutoxybenzoic acid. After adding 0.41 ml of oxalyl chloride and 20 μl of N,N-dimethylformamide successively at ambient temperature, the mixture thus obtained is stirred at ambient temperature for one hour. Then, 1.06 g of aluminum chloride and 1.15 g of 1,3-diisobutoxybenzene are successively added at 5-10° C., and the mixture is stirred at the same temperature as above for one hour. The reaction mixture is added to a mixture of methylene chloride and ice water, and the organic layer is separated. The organic layer is successively washed with water and saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. The residue thus obtained is purified by silica gel column chromatography [eluent; n-hexane:ethyl acetate=5:1] to obtain 1.24 g of 5-(2,4-diisobutoxybenzoyl)-2-isobutoxyphenyl acetate as a yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-ea17877cfbc14e52943175709ae06e5a
Source noteuspto-grants-2008_01