HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388847Generated: November 2, 2026
3-(Trifluoromethyl)phenol → m-Trifluoromethylphenyl 1-amidino-4-piperidinepropionate hydrochloride
https://huagongshe.com/reaction/1388847
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Trifluoromethyl)phenol | HCID 7376 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Amidino-4-piperidinepropionic acid hydrochloride | HCID 15583512 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | m-Trifluoromethylphenyl 1-amidino-4-piperidinepropionate hydrochloride | HCID 70508313 | 62.1% |
Reaction Steps
A mixture of 4.0 g of 1-amidino-4-piperidinepropionic acid hydrochloride and 2.75 g of m-trifluoromethylphenol was suspended in 27 ml of dry pyridine. To the suspension was added 3.5 g of dicyclohexylcarbodiimide, and the resulting mixture was stirred at room temperature for 6 hours. After removal of any insoluble materials, the solvent was removed. The residue was washed with ether, dissolved in chloroform and then stirred. After removal of any insoluble materials, the filtrate was washed twice with a saturated sodium chloride solution and then dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to obtain 4.0 g (yield: 62.0%) of m-trifluoromethylphenyl 1-amidino-4-piperidinepropionate hydrochloride as colorless crystals having a melting point of 97° to 100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04433152 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-cd0940ffb03942e794163208124b35a5 |
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| Source note | uspto-grants-1984_02 |
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