HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154579Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 178512132, compound
https://huagongshe.com/reaction/1154579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 54417104 | HCID 54417104 | — |
| Reactant | HCID 178523389 | HCID 178523389 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178512132 | HCID 178512132 | 76.3% |
Reaction Steps
To a solution of 5.0 g of trans-4-benzyloxycarbonylaminomethylcyclohexanecarboxylic acid in 50 ml of dried pyridine, while being cooled in ice, was added 4.2 g of DCC. After 30 minutes of stirring, to the mixture was added 4.4 g of 4-(β-amidinoethenyl)phenol methanesulfonate. The mixture was stirred overnight at room temperature. The DCU precipitated from the reaction mixture was separated by filtration and washed with pyridine. Ethyl ether was added to the combined filtrate to precipitate a white substance which was collected by filtration, washed with ethyl ether, and recrystallized from ethanol to yield 5.7 g of colorless needle crystals of 4-(β-amidinoethenyl)pnenyl trans-4-benzyloxycarbonylaminomethylcyclohexanecarboxylate methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04490388 |
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| Source dataset | uspto-grants-1984_12 |
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| ORD ID | ord-c75e7b4dc30b41838228de3f2421fa46 |
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| Source note | uspto-grants-1984_12 |
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