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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 850899생성일: 2026년 10월 25일

Trimethylamine oxide → 2-(3-Fluoropropyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

https://huagongshe.com/reaction/850899

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참여 물질

역할이름HCID투입량
반응물Trimethylamine oxideHCID 1145—
반응물PinacolHCID 6425—
반응물CyclohexeneHCID 8079—
반응물3-FluoropropeneHCID 69958—
반응물(Dimethyl sulfide)trihydroboronHCID 12423031—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-(3-Fluoropropyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 1936469835.5%

반응 조건

온도0 °C

반응 단계

2.5 ml (25 mmol) of borane-dimethyl sulphide (1:1) complex were dissolved in 50 ml of dimethoxyethane and the solution was cooled to 0° C. under nitrogen. 5.3 ml (52.5 mmol) of cyclohexene were then added. The solution was stirred at 0° C. for 15 minutes, then at room temperature for 1 hour and then cooled to -10° C. 1.6 g (27 mmol) of 3-fluoropropene were condensed and then added to the foregoing solution which was then stirred at room temperature under a dry ice condenser. After 1 hour the condenser was removed and stirring was continued for a further 1 hour. 3.9 g (52 mmol) of trimethylamine N-oxide were added and the solution was stirred for 1 hour. 3.1 g (26.3 mmol) of 2,3-dimethyl-2,3-butanediol were added and the solution was stirred for 16 hours. The solution was evaporated and the residue was distilled. The distillate boiling at 35-65° C./1mm Hg was collected and purified by chromatography on silica gel using diethyl ether/ hexane (1:9) for the elution to give 1.67 g of 4,4,5,5-tetramethyl-2-(3-fluoropropyl)-1,3,2-dioxaborolane as a colourless oil; 1H NMR (250 MHz, CDCl3) δ: 0.75-0.85 (m, 2H), 1.25 (s, 12H), 1.7-1.9 (m, 2H), 4.28 (t, 1H), 4.48 (t, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06018020
출처 데이터셋uspto-grants-2000_01
ORD IDord-0554b68956574eb2ae155f537052c023
출처 메모uspto-grants-2000_01