Vinylidene fluoride → 8-(2,2,2-Trifluoroethylidene)-1,4-dioxaspiro[4.5]decane
반응식
[F:1][C:2]([F:4])=[CH2:3].[Li]C(CC)C.[O:10]1[C:14]2([CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[O:13][CH2:12][CH2:11]1.[Cl-].[NH4+].CCN(S(F)(F)[F:28])CC>C(Cl)Cl.C(OCC)C.O1CCCC1>[F:1][C:2]([F:28])([F:4])[CH:3]=[C:17]1[CH2:18][CH2:19][C:14]2([O:13][CH2:12][CH2:11][O:10]2)[CH2:15][CH2:16]1참가 물질
반응물 5
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- -100 °C
실험 절차
At −100° C., 22 g of 1,1-difluoroethylene were condensed into a solvent mixture of 400 ml of tetrahydrofuran and 100 ml of diethyl ether. Subsequently, 153 ml of a 1.3 molar solution of sec-BuLi were added dropwise to the reaction solution at a temperature between −90° C. and −100° C. Finally, 31.2 g of 1,4-dioxaspiro[4.5]decane were added, the solution was stirred at −100° C. for another 20 minutes and subsequently warmed to 0° C. with stirring. The reaction solution was poured into an aqueous ammonium chloride and extracted with methylene chloride and the combined organic phases were dried over magnesium sulfate and concentrated. The residue was taken up in 400 ml of methylene chloride and, at −70° C., reacted with 32 g (0.2 mol) of DAST, dissolved in 100 ml of methylene chloride. The mixture was then slowly warmed to 0° C. with stirring, and the reaction solution was subsequently poured into an aqueous ammonium chloride. The product was extracted with diethyl ether and the combined organic phases were dried over MgSO4 and concentrated. The residue was chromatographed over silica gel (petroleum ether/ethyl acetate 4:1), to give the title product as a colourless oil.
후처리
- customAt −100° C.
- customcondensed
- temperaturesubsequently warmed to 0° C.
- stirringwith stirring
- extractionextracted with methylene chloride
- dry with materialthe combined organic phases were dried over magnesium sulfate
- concentrationconcentrated
- customwas taken up in 400 ml of methylene chloride and, at −70° C.
- temperatureThe mixture was then slowly warmed to 0° C.
- stirringwith stirring
- extractionThe product was extracted with diethyl ether
- dry with materialthe combined organic phases were dried over MgSO4
- concentrationconcentrated
- customThe residue was chromatographed over silica gel (petroleum ether/ethyl acetate 4:1)
출처 및 근거
- ORD 기록
- ord-06c96a7b378a45e7b9a3621bb1afbcb6
- 출처 데이터셋
- uspto-grants-2001_03
- 특허 번호
- US06197729B1
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