HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642944Generated: October 30, 2026
2,2,2-Trifluoroethanol → HCID 15605820, compound
https://huagongshe.com/reaction/642944
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | 4-Phenylbenzylamine | HCID 344989 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15605820 | HCID 15605820 | — |
Reaction Steps
0.119 ml (1.64 mmol) of 2,2,2-trifluoroethanol and 0.306 ml (1.49 mmol) of N,N-diisopropylethylamine are added, dropwise and at ambient temperature, to a solution of 0.3 g (1.49 mmol) of para-nitrophenyl chloroformate in 15 ml of methylene chloride. The mixture is stirred at ambient temperature for 2 h, and then 0.275 g (1.5 mmol) of 4-phenylbenzylamine is added. N,N-Diisopropylethylamine is subsequently added, dropwise and at ambient temperature, until the precipitate which has formed disappears. The transparent solution thus obtained is stirred at ambient temperature for 1 h. The reaction medium is diluted with a further 10 ml of methylene chloride and washing is carried out with a saturated aqueous ammonium chloride solution and with a saturated aqueous sodium chloride solution. The phases are separated and the organic phase is dried over sodium sulfate. The product is filtered, the filtrate is concentrated under reduced pressure and the residue is purified by silica gel chromatography with methylene chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696374B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-ede7f830aa0040aaad7cb02d9eee2dd9 |
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| Source note | uspto-grants-2010_04 |
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