HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476541Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 178477423, compound
https://huagongshe.com/reaction/476541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-ethyl-1H-pyrazol-5-ol | HCID 10313108 | — |
| Reactant | 2-Chloro-3-ethylthiomethyl-4-methanesulfonylbenzoic acid | HCID 15132840 | — |
| Solvent | 2-Methyl-2-butanol | HCID 6405 | — |
| Product | HCID 178477423 | HCID 178477423 | — |
Reaction Steps
3 g of 2-chloro-3-ethylthiomethyl-4-methanesulfonylbenzoic acid, 0.72 g of potassium carbonate, 50 ml of t-amyl alcohol, 1.95 g of N,N'-dicyclohexylcarbodiimide and 4.5 g of a 25% t-amyl alcohol solution of 1-ethyl-5-pyrazolone were mixed and heated under stirring for 4 hours at a temperature of from 70° to 80° C. After cooling, the mixture was distilled under reduced pressure, and 200 ml of water was added to the residue. After filtering off the insolubles, the filtrate was washed with chloroform. Hydrochloric acid was added to the aqueous layer, and the mixture was extracted with chloroform. The extract was dried, and the solvent was distilled off to obtain the desired product as a crude product. The crude product was recrystallized from ethanol to obtain 1.88 g of the purified product. (Melting pont: 142°-145° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04885022 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-355a142f03664f42bb8b4d5469b9d1bc |
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| Source note | uspto-grants-1989_12 |
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