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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 504979생성일: 2026년 10월 25일

E-methyl 6,6,6-trifluoro-5-hydroxy-5-(trifluoromethyl)hex-2-enoate → Methyl 6,6,6-trifluoro-5-hydroxy-5-(trifluoromethyl)hexanoate

https://huagongshe.com/reaction/504979

반응식

참여 물질

역할이름HCID투입량
반응물E-methyl 6,6,6-trifluoro-5-hydroxy-5-(trifluoromethyl)hex-2-enoateHCID 59429090—
촉매PalladiumHCID 23938—
용매Ethyl AcetateHCID 8857—
생성물Methyl 6,6,6-trifluoro-5-hydroxy-5-(trifluoromethyl)hexanoateHCID 5942908791%

반응 단계

To a 330 mL thick-walled glass hydrogenation vessel was added 37.7 g E-methyl 6,6,6-trifluoro-5-hydroxy-5-(trifluoromethyl)hex-2-enoate (I) (141 mmol), 0.5 g palladium-on-carbon (5 wt % Pd), and 150 mL ethyl acetate. The reaction vessel was attached to a Parr hydrogenation apparatus and the reaction solution degassed via three successive pump-backfill cycles with nitrogen. The reaction vessel was pressurized to 40 psi with hydrogen and shaken at room temperature for 20 hours, after which the pressure had fallen to 34 psi. The excess hydrogen was removed via three successive pump-backfill cycles with nitrogen and the palladium catalyst removed via filtration through 1.0 micron glass fiber and 0.2 micron PTFE filters. The solvent was removed in vacuo and the crude reaction mixture distilled under vacuum (6 Torr, 64-74° C.) to afford 34.4 g (91%) of methyl 6,6,6-trifluoro-5-hydroxy-5-(trifluoromethyl)hexanoate (II) as a colorless liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07781157B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-34836a414c9c4e2c83e08b6b670887c8
출처 메모uspto-grants-2010_08