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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2216009생성일: 2026년 10월 25일

Triethylamine → 2,2,2-Trifluoro-1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)phenyl)ethanol

https://huagongshe.com/reaction/2216009

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
반응물3'-Bromo-2,2,2-trifluoroacetophenoneHCID 14647442—
촉매HCID 178418476HCID 178418476—
생성물2,2,2-Trifluoro-1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)phenyl)ethanolHCID 2188615553%

반응 조건

온도95 °C

반응 단계

To an oven-dried round bottom flask fitted with a stir bar and a rubber septum was added 1-(3-bromo-phenyl)-2,2,2-trifluoro-ethanone (560 mg, 2.2 mmol, as prepared in Example 28, step a), 4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (0.96 mL, 6.6 mmol, Aldrich Chemical Company), (PPh3)2PdCl2 (93 mg, 0.132 mmol, Strem Chemicals, Inc., Newburyport, Mass.), and Et3N (1.8 mL, 13.2 mmol). The reaction mixture was evacuated, purged with argon, and then suspended in dioxane (16 mL). After stirring for 18 hr at 95° C., the reaction was allowed to cool and then filtered through Celite.® The filtrate was concentrated in vacuo and the residue was purified by chromatography (SiO2, flash elution: 5% EtOAc in hexanes) to give 350 mg (53%) of an oil that was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07109354B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-1c111f7200ef44e287b880dfd8f2178d
출처 메모uspto-grants-2006_09