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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682158Generated: October 25, 2026

Dicyclohexylcarbodiimide → HCID 178463120, compound

https://huagongshe.com/reaction/1682158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methanesulfonyl-3-methoxycarbonyl-2-methylbenzoic acidHCID 15623657—
ReactantHCID 178418331HCID 178418331—
Solvent2-Methyl-2-butanolHCID 6405—
ProductHCID 178463120HCID 17846312062%

Reaction Steps

1.12 g (0.01 mol) of 1-ethyl-5-hydroxypyrazole was dissolved in 30 ml of t-amyl alcohol, and 2.72 g (0.01 mol) of 4-methanesulfonyl-3-methoxycarbonyl-2-methylbenzoic acid, 2.27 g (0.011 mol) of N,N'-dicyclohexylcarbodiimide and 0.76 g (0.0055 mol) of anhydrous potassium carbonate were sequentially added thereto. The mixture was reacted at 80° C. for 6 hours under stirring. After completion of the reaction, t-amyl alcohol was distilled off under reduced pressure, and then water was added to the residue to dissolve the soluble component. The mixture was subjected to filtration to separate out the insolubles. The aqueous solution thus obtained was washed twice with chloroform, and then concentrated hydrochloric acid was added to adjust pH<1. The precipitated oil component was extracted with chloroform. The chloroform layer was washed sequentially with water and a saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure, and the residue thus obtained was recrystallized from water/ethanol to obtain 2.26 g of the desired product. (Yield: 62%, melting point: 150°-152° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175299
Source datasetuspto-grants-1992_12
ORD IDord-b03e6b725bb5445d890de8631c03b832
Source noteuspto-grants-1992_12