HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709346Generated: October 25, 2026
Dicyclohexylcarbodiimide → HCID 178463120, compound
https://huagongshe.com/reaction/1709346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methanesulfonyl-3-methoxycarbonyl-2-methylbenzoic acid | HCID 15623657 | — |
| Reactant | HCID 178418331 | HCID 178418331 | — |
| Solvent | 2-Methyl-2-butanol | HCID 6405 | — |
| Product | HCID 178463120 | HCID 178463120 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04948887 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-5aa39d87d3ed41d9adb5a86d20c8a5ed |
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| Source note | uspto-grants-1990_08 |
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