HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987028Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 86600355, compound
https://huagongshe.com/reaction/987028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 3-(3,5-Ditert-butyl-4-hydroxyphenyl)prop-2-enoic acid | HCID 99819 | — |
| Reactant | 4-Amino-2-Nitrophenol | HCID 3417419 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86600355 | HCID 86600355 | 73.9% |
Reaction Steps
1.78 g (6.4 mmoles) of 3,5-di-tert-butyl-4-hydroxycinnamic acid, 0.99 g (6.4 mmoles) of 4-amino-2-nitrophenol, previously diluted in 10 ml of DMF, 0.86 g (6.4 mmoles) of hydroxybenzotriazol and 1.32 g (6.4 mmoles) of dicyclohexylcarbodiimide are introduced into a 50 ml flask containing 10 ml of THF. The reaction medium is agitated for 15 hours at ambient temperature, the precipitate which appears is filtered and rinsed with ethyl acetate. After concentration of the solution under reduced pressure, the residue is diluted in 20 ml of ethyl acetate and the insoluble part is filtered again. The filtrate is washed with 20 ml of a saturated solution of sodium carbonate followed by 20 ml of water and 20 ml of a saturated solution of sodium chloride. After drying over sodium sulphate, the organic solution is filtered and concentrated to dryness under reduced pressure. The residue is purified on a silica column (eluant: heptane/ethyl acetate: 8/2). The pure fractions are collected and concentrated under vacuum to produce 1.95 g (47%) of the expected compound in the form of a yellow-orange powder. Melting point: 231-232° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06630461B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-d88c2478d7c24955a2dfcefdb80a95bc |
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| Source note | uspto-grants-2003_10 |
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