Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400093Generated: October 26, 2026

Dimethylformamide → N,N'-Dicyclohexylurea

https://huagongshe.com/reaction/400093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1,5-Diphenylpyrazolidin-3-oneHCID 3695373—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
ProductN,N'-DicyclohexylureaHCID 4277—

Reaction Steps

Into 100 ml of dimethylformamide, 23.8 g of Compound (A), 30.1 g of Compound (B) and 0.8 g of 4-dimethylamino-pyridine were dissolved, and thereto an ethyl acetate 20 ml solution containing 20.6 g of dicyclohexylcarbodiimide was added dropwise in an ice bath. After the dropwise addition, the solution was allowed to react at room temperature over night. Into the reaction solution, 200 ml of ethyl acetate was poured, and dicyclohexylurea obtained was separated by filtration. Into the filtrate, 300 ml of water was poured to perform liquid separation operation. Water washing was performed twice, the organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and the oily product obtained was subjected to silica gel column chromatography. As a result, from the methylene chloride/ethyl acetate=10/3 fraction, 43 g of Compound (C) was obtained as a pale yellow oily product. ##STR16## Synthesis of Compound (D):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05827637
Source datasetuspto-grants-1998_10
ORD IDord-46a28bea654e4c7d9fedeb6812c1b619
Source noteuspto-grants-1998_10