HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258150Generated: October 26, 2026
2,2,3,3-Tetrafluoro-1-propanol → Methyl 2,2,3,3-tetrafluoropropyl carbonate
https://huagongshe.com/reaction/2258150
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2,3,3-Tetrafluoro-1-propanol | HCID 6441 | — |
| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Catalyst | Sodium methanolate methanol | HCID 23694274 | — |
| Product | Methyl 2,2,3,3-tetrafluoropropyl carbonate | HCID 21263425 | 49% |
Reaction Steps
In a flask (500-ml volume) equipped with 10 distillation columns, 2,2,3,3-tetrafluoropropanol (100 g, 0.76 mol), dimethyl carbonate (205 g, 2.3 mol) and a 28% sodium methoxide/methanol solution (1.4 g) were charged. The flask was heated to 120° C. to allow the starting materials to react for 10 hours while removing the methanol from the distillation columns by evaporation. After allowing the mixture to cool to room temperature, an aqueous solution of ammonium chloride was added to the mixture and the mixture was shaken to remove the sodium methoxide. The organic layer was washed with water, dried and distilled to give methyl 2,2,3,3-tetrafluoropropyl carbonate as a colorless liquid (70 g, yield 49%). The chemical structure of the produced compound was determined based on the IR and NMR absorbance spectra shown in FIG. 9 and FIG. 10 respectively and the mass spectrometry spectrum (M/e=190).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05659062 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-fdbf290609274e98a2512a70ce40f256 |
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| Source note | uspto-grants-1997_08 |
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