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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249639Generated: October 29, 2026

Dimethylformamide → HCID 68987739, compound

https://huagongshe.com/reaction/2249639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
ReactantHCID 17816566HCID 17816566—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 68987739HCID 6898773983.9%

Reaction Steps

In 40 ml of tetrahydrofuran is dissolved 4.00 g of 5-(2,4-diisobutoxybenzoyl)-2-isobutoxybenzoic acid, to which are added 0.95 ml of oxalyl chloride and 20 μl of N,N-dimethylformamide. The mixture thus obtained is stirred at ambient temperature for one hour. To the reaction mixture are added 3.03 g of glycine ethyl ester hydrochloride and 4.2 ml of triethylamine successively, and the mixture thus obtained is stirred for one hour under reflux with heating. The reaction mixture is cooled to ambient temperature, chloroform and water are added, and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride successively 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; hexane:ethyl acetate=2:1) to obtain 4.00 g of ethyl 2-{[5-(2,4-diisobutoxybenzoyl)-2-isobutoxybenzoyl]amino}acetate as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-b412c9130f3146498f64a5d5ee0a6a25
Source noteuspto-grants-2008_01