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Triethylsilane → 1-Bromo-4-cyclobutylbenzene

HRID 2244307
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HRID 2244307 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2(O)[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.C([SiH](CC)CC)C>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 12052TriethylsilaneHCID 120954191-(4-Bromophenyl)cyclobutanol

생성물 1

HCID 571850921-Bromo-4-cyclobutylbenzene수율 66.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
-78 °C

실험 절차

To a solution of 1.37 g of 1-(4-bromophenyl)-cyclobutanol (6 mmol) in 15 ml DCM were added 1.15 ml of triethylsilane (7.2 mmol) and the mixture was cooled to −78° C. Then 1.15 ml of boron trifluoride diethyl etherate complex were added and the reaction mixture was warmed to −40° C. and stirred for 8 h. The reaction was then quenched by addition of 10% aqueous KHCO3 and the mixture was extracted three times with DCM. The combined extracts were washed with brine, dried with magnesium sulfate and concentrated. The remaining residue was purified by column chromatography (silica gel; cyclohexane) to give 0.84 g (66%) of 1-bromo-4-cyclobutyl-benzene as a colorless liquid. 1H NMR (CDCl3, 300 MHz): δ 1.85 (m, 1H), 1.92-2.18 (m, 3H), 2.33 (m, 2H), 3.49 (quint, J=8.5 Hz, 1H), 7.08 (d, J=8.5 Hz, 2H), 7.40 (d, J=8.5 Hz, 2H).

후처리

  1. additionThen 1.15 ml of boron trifluoride diethyl etherate complex were added
  2. temperaturethe reaction mixture was warmed to −40° C.
  3. customThe reaction was then quenched by addition of 10% aqueous KHCO3
  4. extractionthe mixture was extracted three times with DCM
  5. washThe combined extracts were washed with brine
  6. dry with materialdried with magnesium sulfate
  7. concentrationconcentrated
  8. customThe remaining residue was purified by column chromatography (silica gel; cyclohexane)

출처 및 근거

ORD 기록
ord-65462d6a3d8a45139b23fa431cf26929
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07678818B2

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