HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393843Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 21918641, compound
https://huagongshe.com/reaction/393843
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 3,5-Di-tert-butyl-4-hydroxybenzoic acid | HCID 15007 | — |
| Reactant | 1-(4-Nitrophenyl)piperazine | HCID 80447 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21918641 | HCID 21918641 | 89% |
Reaction Steps
2.07 g (10 mmoles) of 1-(4-nitrophenyl)piperazine, 2.5 g (10 mmoles) of 3,5-di-tert-butyl-4-hydroxybenzoic acid and 2.26 g (11 mmoles) of dicyclohexylcarbodiimide are introduced into a 100 ml flask containing 25 ml of DMF. The reaction medium is agitated for 15 hours at ambient temperature, the precipitate which appears is filtered out and rinsed with ethyl acetate. After concentration of the filtrate under reduced pressure, the residue is diluted in 20 ml of ethyl acetate and a new insoluble is eliminated by filtration. The solvent is evaporated off under vacuum and the residue is precipitated from diethyl ether. The solid is filtered, rinsed with 2×20 ml of ethyl acetate in order to obtain a yellow powder with a yield of 89%. Melting point: 159.5-160.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809088B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-580fa4b0192e4ef98f960196d3e7ba33 |
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| Source note | uspto-grants-2004_10 |
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