HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781228Generated: October 29, 2026
2,2,2-Trifluoroethanol → Methyl 2,2,2-trifluoroethyl carbonate
https://huagongshe.com/reaction/1781228
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Catalyst | Sodium methanolate methanol | HCID 23694274 | — |
| Product | Methyl 2,2,2-trifluoroethyl carbonate | HCID 17761042 | 33% |
Reaction Steps
In a flask (3-liter volume) equipped with 10 distillation columns, 2,2,2-trifluoroethanol (790 g, 7.9 ml), dimethyl carbonate (2140 g, 23.7 mol) and a 28% sodium methoxide/methanol solution (15.3 g) were charged. The flask was heated to 100° C. to allow the starting materials to react for 30 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 2,2,2-trifluoroethyl carbonate as a colorless liquid (410 g, yield 33%). The chemical structure of the produced compound was determined based on the IR and NMR absorbance spectra shown in FIG. 3 and FIG. 4 respectively and the mass spectrometry spectrum (M/e=158).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05633099 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-c04ca43d5701435492ee6ef93800bddf |
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| Source note | uspto-grants-1997_05 |
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