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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769677Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 20096977, compound

https://huagongshe.com/reaction/1769677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant1,2-Bis(4-ethylphenyl)-2-hydroxyethanoneHCID 15044204—
ReactantHCID 20096955HCID 20096955—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 20096977HCID 2009697727.5%

Reaction Steps

1,3-Dicyclohexylcarbodiimide (DCC; 0.81 g, 3.92 mmol) was added in one portion to a rapidly-stirred mixture of 4-[[[(2,6-dimethylphenyl)amino]carbonyl]methyl]-1-piperazineacetic acid (1.0 g, 3.27 mmol), 2-hydroxy-1,2-di-(4-ethylphenyl)ethanone (IX; 0.88 g, 3.27 mmol) and dimethylaminopyridine (DMAP: 40 mg) in anhydrous dimethylformamide (25 mL). After 2 hours at ambient temperature, an additional equivalent of DCC and DMAP were added. The mixture was stirred further for 22 hours at room temperature before it was heated to 70° C. for 6 hours. Upon cooling, the mixture was diluted with ethyl acetate, washed with saturated sodium bicarbonate solution and brine, dried and concentrated. Purification of the residue by flash chromatography on silica gel (gradient elution with 50% ethyl acetate in hexanes followed by ethyl acetate) afforded 0.50 g of the benzoin ester product (VI) as an off-white solid. The ester was used in subsequent reactions without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382584
Source datasetuspto-grants-1995_01
ORD IDord-2b6067b4442849ffa4efd1ab5df8312c
Source noteuspto-grants-1995_01