HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058937Generated: November 2, 2026
Dicyclohexylcarbodiimide → HCID 12773843, compound
https://huagongshe.com/reaction/2058937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 12773838 | HCID 12773838 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12773843 | HCID 12773843 | — |
Reaction Steps
The compound produced in Example 2 is dissolved in about 500 milliliters methylene chloride and the solution is chilled under nitrogen to 15° C. in a dry ice-acetone mixture. 4-Dimethylaminopyridine is added and the mixture is stirred for five minutes. A slight excess of dicyclohexylcarbodiimide dissolved in methylene chloride is added with stirring. The chilled source is removed after 15 minutes and the solution is stirred overnight at room temperature. The volume of the reaction mixture is reduced on a rotary evaporator under reduced pressure to about 100 milliliters. A precipitate is removed by filtration and the filter residue is washed several times with methylene chloride. The filtrate and combined washings are washed successively with 1N HCl, saturated aqueous NaHCO3, water and saline and the solution is dried over MgSO4. Evaporation of the methylene chloride with a rotary evaporator under reduced pressure yields the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04320057 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-a38f20e1ba75411ba341261454f0ca79 |
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| Source note | uspto-grants-1982_03 |
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