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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461499Generated: November 1, 2026

Dicyclohexylcarbodiimide → HCID 19979937, compound

https://huagongshe.com/reaction/1461499

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 numberUS05075032
Source datasetuspto-grants-1991_12
ORD IDord-ec2a63b8a5174598b8646f3945fc40d6
Source noteuspto-grants-1991_12