HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477296Generated: October 29, 2026
Dicyclohexylcarbodiimide → HCID 19979937, compound
https://huagongshe.com/reaction/477296
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Iodoheptane | HCID 20274 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 4'-(Heptyloxy)[1,1'-biphenyl]-4-carboxylic acid | HCID 4433908 | — |
| Reactant | HCID 19979915 | HCID 19979915 | — |
| Reactant | HCID 178511285 | HCID 178511285 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19979937 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886620 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-476f865ede454ea795b872dd43e935ed |
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| Source note | uspto-grants-1989_12 |
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