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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373738Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 21918641, compound

https://huagongshe.com/reaction/2373738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3,5-Di-tert-butyl-4-hydroxybenzoic acidHCID 15007—
Reactant1-(4-Nitrophenyl)piperazineHCID 80447—
SolventDimethylformamideHCID 6228—
ProductHCID 21918641HCID 2191864189%

Reaction Steps

2.07 g (10 mmoles) of 1-(4-nitrophenyl)piperazine, 2.5 cg (10 mmoles) of 3,5-di-tert-butyl-4-hydroxybenzoic acid and 2.26 g (11 mmoles) of dicyclohexylcarbodiimide are introduced into a 100 ml flask containing 25 ml of DMF. The reaction medium is agitated for 15 hours at ambient temperature, the precipitate which appears is filtered out and rinsed with ethyl acetate. After concentration of the filtrate under reduced pressure, the residue is diluted in 20 ml of ethyl acetate and a new insoluble is eliminated by filtration. The solvent is evaporated off under vacuum and the residue is precipitated from diethyl ether. The solid is filtered, rinsed with 2×20 ml of ethyl acetate in order to obtain a yellow powder with a yield of 89%. Melting point: 159.5-160.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459558B2
Source datasetuspto-grants-2008_12
ORD IDord-593008ecd1d74988af9a3bac000d6972
Source noteuspto-grants-2008_12