HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359624Generated: October 29, 2026
Iodopentafluoroethane → HCID 10400765, compound
https://huagongshe.com/reaction/1359624
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodopentafluoroethane | HCID 9636 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 4-Tert-Butylaniline | HCID 69861 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Bis(tetrabutylammonium) sulphate | HCID 11433187 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10400765 | HCID 10400765 | 18% |
Reaction Steps
To a liquid mixture of 40 ml of water and 40 ml of ethyl acetate were successively added 2.2 g of 4-tert-butylaniline, 5.0 g of perfluoroethyl iodide, 3.1 g of sodium dithionite, 1.5 g of sodium hydrogen carbonate and 0.6 g of tetrabutylammonium sulfate, and the resulting mixture was stirred at room temperature for 15 hours. The organic layer was separated, then the aqueous layer was extracted with 20 ml of ethyl acetate, and the organic layer were combined and washed successively with 2N aqueous hydrochloric acid, 5% aqueous sodium carbonate solution and saturated aqueous sodium chloride solution. The organic layer was dried with magnesium sulfate, then filtered, the organic solvent was distilled off under reduced pressure and the residue was purified by column chromatography to obtain 0.7 g of the intended product. Yield: 18%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06600074B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-43508cab97bb47688eacc503970a1322 |
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| Source note | uspto-grants-2003_07 |
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