HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682157Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 178463118, compound
https://huagongshe.com/reaction/1682157
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 14721238 | HCID 14721238 | — |
| Reactant | HCID 178418331 | HCID 178418331 | — |
| Solvent | 2-Methyl-2-butanol | HCID 6405 | — |
| Product | HCID 178463118 | HCID 178463118 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05175299 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-62aadf5f7be14e159cb9a28356e84aa6 |
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| Source note | uspto-grants-1992_12 |
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