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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1611730생성일: 2026년 10월 25일

Trifluoroacetic acid → 5,7-Bis(1,1-dimethylethyl)-3-phenyl-(3H)-benzofuran-2-one

https://huagongshe.com/reaction/1611730

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물HCID 54208733HCID 54208733—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물5,7-Bis(1,1-dimethylethyl)-3-phenyl-(3H)-benzofuran-2-oneHCID 645535690%

반응 조건

온도80 °C

반응 단계

A solution of 589 mg (2.0 mmol) of a mixture of 6-benzylidene-2,4-di-tert-butyl-cyclohexa-2,4-dienone (compound (302), Table 3) and the corresponding dimer (compound (402), Table 4), prepared according to Example 2b, in 7 ml of toluene is degassed using argon and then 58 mg (0.05 mmol) of tetrakis(triphenylphosphine)palladium(0) and 23 mg (0.20 mmol) of trifluoroacetic acid are added. The autoclave is flushed with carbon monoxide and sealed, and a carbon monoxide pressure of 5 bar is then applied. The reaction mixture is maintained at 80° C. for 20 hours. After cooling to room temperature, the reaction mixture is poured into water and extracted three times using ethyl acetate. The organic phases are combined, dried over sodium sulfate and concentrated using a vacuum rotary evaporator. Crystallisation of the residue from isopropanol yields 580 mg (90%) of 5,7-di-tert-butyl-3-phenyl-3H-benzofuran-2-one (compound (102), Table 1), m.p. 116-119° C. Analysis, calculated: C 81.95; H 8.13%. Analysis, found: C 81.93; H 8.13%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06989446B2
출처 데이터셋uspto-grants-2006_01
ORD IDord-7fb6dfad001e4eb289da315bb5973d59
출처 메모uspto-grants-2006_01