참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 2,2,3,3-Tetrafluoro-1-propanol | HCID 6441 | — |
| 반응물 | Methyl chloroformate | HCID 6586 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | Methyl 2,2,3,3-tetrafluoropropyl carbonate | HCID 21263425 | 87.3% |
반응 단계
Methyl chloroformate (130 mL, 159 g, 1.68 mol) was added slowly over a period of 3 h 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 (U.S. Pat. No. 5,659,062).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08530099B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-d8af474a27ac44c495844351bcdec7fb |
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| 출처 메모 | uspto-grants-2013_09 |
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