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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227884Generated: October 31, 2026

Bis(4-chlorophenyl)acetic acid → HCID 18475024, compound

https://huagongshe.com/reaction/2227884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(4-chlorophenyl)acetic acidHCID 6730—
Reactant2-(Methylamino)ethanolHCID 8016—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 18475024HCID 1847502486.4%

Reaction Steps

A suspension of the bis(4-chlorophenyl)acetic acid (10.40 g, 36.99 mmol) in dichloromethane (100 ml) was treated with oxalyl chloride (6.2 ml, 71.07 mmol) and dimethylformamide (1 drop). The mixture was stirred at room temperature overnight and was then concentrated under vacuum and coevaporated with toluene. The residue was dissolved in tetrahydrofuran (50 ml) and this solution was added to a mixture of 2-(methylamino)ethanol (6.0 ml, 74.7 mmol) in tetrahydrofuran (100 ml), water (50 ml) and sodium bicarbonate (10 g). The reaction was stirred at room temperature for 1 hour, then diluted with ethyl acetate. This was washed with water, HCl 1N, saturated sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, filtered and concentrated. The residual white solid was crystallized from ethyl acetate to give the title compound (10.81 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414179B1
Source datasetuspto-grants-2002_07
ORD IDord-26afb04e619f4cd6947fd33a9aa24ab9
Source noteuspto-grants-2002_07