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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 476539Erstellt: 26. Oktober 2026

Dicyclohexylcarbodiimide → HCID 178463120, Verbindung

https://huagongshe.com/reaction/476539

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
EduktPotassium CarbonateHCID 11430—
Edukt4-Methanesulfonyl-3-methoxycarbonyl-2-methylbenzoic acidHCID 15623657—
EduktHCID 178418331HCID 178418331—
Lösungsmittel2-Methyl-2-butanolHCID 6405—
ProduktHCID 178463120HCID 17846312062%

Reaktionsschritte

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.)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04885022
Quelldatensatzuspto-grants-1989_12
ORD IDord-b3d5f1c796494c3083da92d2106c21cc
Quellennotizuspto-grants-1989_12