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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058937Generated: November 2, 2026

Dicyclohexylcarbodiimide → HCID 12773843, compound

https://huagongshe.com/reaction/2058937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 12773838HCID 12773838—
ReactantAcetone cardiceHCID 18522661—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 12773843HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04320057
Source datasetuspto-grants-1982_03
ORD IDord-a38f20e1ba75411ba341261454f0ca79
Source noteuspto-grants-1982_03