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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133506생성일: 2026년 10월 27일

1,1,1-Trifluoro-2,4-pentanedione → 2,2,2-Trifluoro-1-(2-methyl-4-phenyl-benzo[4,5]thieno[2,3-b]pyridin-3-yl)-ethanone

https://huagongshe.com/reaction/133506

반응식

참여 물질

역할이름HCID투입량
반응물1,1,1-Trifluoro-2,4-pentanedioneHCID 73943—
반응물(2-Amino-benzo[b]thiophen-3-yl)-phenyl-methanoneHCID 68896066—
촉매Sulfuric AcidHCID 1118—
용매Acetic AcidHCID 176—
생성물2,2,2-Trifluoro-1-(2-methyl-4-phenyl-benzo[4,5]thieno[2,3-b]pyridin-3-yl)-ethanoneHCID 1166785017%

반응 조건

온도100 °C

반응 단계

To a stirred solution of 32 mg (0.13 mmol) (2-amino-benzo[b]thiophen-3-yl)-phenyl-methanone (the preparation of which is described in example 11) in 2 ml acetic acid was added 0.016 ml (0.13 mmol) of 1,1,1-trifluoro-pentane-2,4-dione and one drop of sulfuric acid. The mixture was then stirred at 100° C. for 10 minutes in a microwave and then concentrated in vacuo. Flash chromatography (heptane/ethyl acetate 20:1) afforded 8 mg (17%) 2,2,2-trifluoro-1-(2-methyl-4-phenyl-benzo[4,5]thieno[2,3-b]pyridin-3-yl)-ethanone as a light yellow solid. ES-MS m/e (%): 372 (M+H+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390903B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-2b1439634a864ceba4709def4d355351
출처 메모uspto-grants-2008_06