참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Dioxide | HCID 280 | — |
| 반응물 | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Trifluoromethanesulfonyl chloride | HCID 79000 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2,2,2-Trifluoroethyl trifluoromethanesulfonate | HCID 80366 | — |
반응 단계
A solution of trifluoromethanesulfonyl chloride (800 uL, 7.5 mmole) in CH2Cl2 (6 mL) was cooled under argon to -60° C. (IPA:dry ice bath). 2,2,2-Trifluoroethanol was added (456 uL, 6 mmol) and triethylamine (1.04 uL, 7.5 mmol) was added dropwise. The reaction was stirred for 1.5 hours then warmed to 0° C. for 1 hour. Anhydrous ether (20 mL) was added and the mixture was stirred at 0° C. for 30 minutes. The solids were filtered off and the solvent was removed under reduced pressure with the flask maintained at 0° C. This afforded the 2,2,2-trifluoroethyltriflate as a yellow oil which was used immediately.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05726172 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-c1eb50330c204669ac80b93517bb8dec |
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| 출처 메모 | uspto-grants-1998_03 |
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