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Boron trifluoride etherate → 2-(o-Tolyl)cyclohexanol

HRID 2218557
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HRID 2218557 반응식
Br[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[CH:3]=1.[Li]CCCC.[CH:14]12[O:20][CH:19]1[CH2:18][CH2:17][CH2:16][CH2:15]2.B(F)(F)F.CCOCC.[Cl-].[NH4+]>C1COCC1>[C:4]1([CH3:8])[CH:5]=[CH:6][CH:7]=[CH:2][C:3]=1[CH:18]1[CH2:17][CH2:16][CH2:15][CH2:14][CH:19]1[OH:20]
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참가 물질

7

반응물 5

HCID 8000Boron trifluoride etherateHCID 9246Cyclohexene oxideHCID 115603-BromotolueneHCID 25517Ammonium ChlorideHCID 178418339Butyllithium

생성물 1

HCID 2513132-(o-Tolyl)cyclohexanol

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

반응 조건

온도
-78 °C

실험 절차

To a solution of 1-bromo-3-methyl-benzene in THF at −78° C., was added dropwise a solution of nBuLi (1.6M in THF, 12.4 ml) and the reaction mixture was stirred at −78° C. for 30 minutes. After such time, 7-oxa-bicyclo[4.1.0]heptane (3.4 g) was added slowly to the reaction mixture followed by the addition of boron trifluoride etherate (2.5 ml). The reaction mixture was stirred at −78° C. for another 2 hours before allowing it to warm up to room temperature. The solution was then treated with solution of ammonium chloride (25 ml), the phases were separated and then extracted twice with ethyl acetate. The combined organic extracts were then washed with water, dried over sodium sulfate and concentrated in vacuo. The residue was then purified by column chromatography to give 2.9 g of (cis/trans) 2-o-tolyl-cyclohexanol MS(EI) 190.1 (M+).

후처리

  1. stirringThe reaction mixture was stirred at −78° C. for another 2 hours
  2. temperatureto warm up to room temperature
  3. customthe phases were separated
  4. extractionextracted twice with ethyl acetate
  5. washThe combined organic extracts were then washed with water
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe residue was then purified by column chromatography

출처 및 근거

ORD 기록
ord-69dee6e1595449b08b1b5be0a4472616
출처 데이터셋
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07411093B2

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