HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027334Generated: October 26, 2026
Hydrochloric Acid → Methyl 2,2,3,3-tetrafluoropropyl carbonate
https://huagongshe.com/reaction/1027334
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,2,3,3-Tetrafluoro-1-propanol | HCID 6441 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Methyl 2,2,3,3-tetrafluoropropyl carbonate | HCID 21263425 | 87.3% |
Reaction Steps
Methyl chloroformate (130 mL, 159 g, 1.68 mol) was added slowly over a period of 3 hours to a solution of 2,2,3,3-tetrafluoropropanol (132 g, 1.00 mol) in pyridine (300 mL, anhydrous) at −10° C. to 0° C. with magnetic stirring. The reaction mixture was stirred at room temperature overnight. Then, the reaction mixture was mixed with 5% HCl (500 mL) and approximately 50 g of ice, and the resulting mixture was extracted three times with 300 mL portions of ether. The combined organic layer was washed three times with 100 mL portions of 5% HCl, followed by two washes with 100 mL portions of 5% sodium carbonate. The organic phase was then dried over anhydrous sodium sulfate. Ether was removed by rotary evaporation. The crude product (approximately 200 g) was distilled, yielding 166 g (87% yield) of pure methyl 2,2,3,3-tetrafluoropropyl carbonate, also referred to herein as “FS-C”. NMR analysis data were consistent with the literature values as reported in U.S. Pat. No. 5,659,062.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735005B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-eb932d356022487ab2ad7da520c33268 |
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| Source note | uspto-grants-2014_05 |
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