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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682157Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 178463118, compound

https://huagongshe.com/reaction/1682157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 14721238HCID 14721238—
ReactantHCID 178418331HCID 178418331—
Solvent2-Methyl-2-butanolHCID 6405—
ProductHCID 178463118HCID 17846311866%

Reaction Steps

1.12 g (0.01 mol) of 1-ethyl-5-hydroxypyrazole is dissolved in 30 ml of t-amyl alcohol, and then 2.59 g (0.01 mol) of 4-methanesulfonyl-3-methoxymethyl-2-methylbenzoic acid, 2.06 g (0.01 mol) of N,N'-dicyclohexylcarbodiimide and 0.69 g (0.005 mol) of anhydrous potassium carbonate were sequentially added thereto. The mixture was reacted at a temperature of from 80° to 90° C. for 8 hours under stirring. After completion of the reaction, t-amyl alcohol was distilled off under reduced pressure, and 30 ml of water was added to the residue to dissolve the soluble components. The mixture was subjected to filtration to separate out the insolubles. The aqueous solution thus obtained was washed with chloroform, and concentrated hydrochloric acid was added to adjust pH<1. The precipitated oil component was extracted with chloroform. The solvent was distilled off under reduced pressure, and the residue was purified with silica gel column chromatography (eluent: ethyl acetate/ethanol=9/1) to obtain 2.3 g of the desired product. (Yield: 66%, melting point: 116°-118° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175299
Source datasetuspto-grants-1992_12
ORD IDord-62aadf5f7be14e159cb9a28356e84aa6
Source noteuspto-grants-1992_12