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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68347생성일: 2026년 10월 25일

Boron trifluoride etherate → Tert-butyl 5,5,5-trifluoropentanoate

https://huagongshe.com/reaction/68347

반응식

참여 물질

역할이름HCID투입량
반응물Boron trifluoride etherateHCID 8000—
반응물Sodium BicarbonateHCID 516892—
반응물Tert-butyl 2,2,2-trichloroethanimidateHCID 2734700—
반응물5,5,5-trifluoropentanoic AcidHCID 2782446—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Tert-butyl 5,5,5-trifluoropentanoateHCID 8667136998.1%

반응 조건

온도0 °C

반응 단계

To a stirred solution of 5,5,5-trifluoropentanoic acid (5 g, 32.0 mmol) in THF (30 mL) and hexane (30 mL) at 0° C., was added tert-butyl 2,2,2-trichloroacetimidate (11.46 mL, 64.1 mmol). The mixture was stirred for 15 min at 0° C. Boron trifluoride etherate (0.406 mL, 3.20 mmol) was added and the reaction mixture was allowed to warm to room temperature overnight. To the clear reaction mixture was added solid NaHCO3 (5 g) and stirred for 30 min. The mixture was filtered through MgSO4 and washed with hexanes (200 mL). The solution was allowed to rest for 45 min, and the resulting solid material was removed by filtering on the same MgSO4 filter again, washed with hexanes (100 mL) and concentrated under reduced pressure without heat. The volume was reduced to about 30 mL, filtered through a clean fritted funnel, washed with hexane (5 mL), and then concentrated under reduced pressure without heat. The resulting neat oil was filtered through a 0.45 μm nylon membrane filter disk to provide tert-butyl 5,5,5-trifluoropentanoate (6.6 g, 31.4 mmol 98% yield) as a colorless oil: 1H NMR (400 MHz, CDCl3) δ ppm 1.38 (s, 9H) 1.74-1.83 (m, 2H) 2.00-2.13 (m, 2H) 2.24 (t, J=7.28 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822454B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-2a9078c6afe84878bf4b0b6bb43b8e34
출처 메모uspto-grants-2014_09