Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477296Generated: October 29, 2026

Dicyclohexylcarbodiimide → HCID 19979937, compound

https://huagongshe.com/reaction/477296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-IodoheptaneHCID 20274—
ReactantLithium diisopropylamideHCID 2724682—
Reactant4'-(Heptyloxy)[1,1'-biphenyl]-4-carboxylic acidHCID 4433908—
ReactantHCID 19979915HCID 19979915—
ReactantHCID 178511285HCID 178511285—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 19979937HCID 19979937—

Reaction Steps

While cooling with ice, 4.54 g of dicyclohexylcarbodiimide in 10 ml of dichloromethane are added dropwise to a mixture of 6.24 g of 4-heptyloxy-4'-biphenylcarboxylic acid, 4.46 g of 4-cyano-4-heptylcyclohexanol [obtainable from trans-4-cyanocyclohexanol by protecting the hydroxyl group as THP ether, reaction with heptyl iodide and lithium diisopropylamide and subsequent cleavage of the protective group] and 0.2 g of 4-N,N'-dimethylaminopyridine in 45 ml of dichloromethane. After 25 hours, the precipitated urea derivative is filtered off by suction, the filtrate is diluted with methylene chloride and washing was carried out several times in sequence with dilute hydrochloric acid and with water. After drying, the removal of the solvent and purification by chromatography and crystallization, 4-cyano-4-heptylcyclohexyl 4-heptyloxy-4'-biphenylcarboxylate is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886620
Source datasetuspto-grants-1989_12
ORD IDord-476f865ede454ea795b872dd43e935ed
Source noteuspto-grants-1989_12