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Hydrogen Bromide → 4-(2-bromoethyl)-1,1-dimethylcyclohexane

HRID 968436
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HRID 968436 반응식
[CH3:1][C:2]1([CH3:11])[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9]O)[CH2:4][CH2:3]1.[BrH:12]>S(=O)(=O)(O)O>[Br:12][CH2:9][CH2:8][CH:5]1[CH2:6][CH2:7][C:2]([CH3:11])([CH3:1])[CH2:3][CH2:4]1
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참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 149767172-(4,4-Dimethylcyclohexyl)ethan-1-ol

생성물 1

HCID 222898944-(2-bromoethyl)-1,1-dimethylcyclohexane

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

반응 조건

온도
90 °C

실험 절차

A mixture of 2-(4,4-dimethylcyclohexyl)ethanol (WO99/59971) (2 g, 12.8 mmol), concentrated sulphuric acid (750 μl) and 48% hydrobromic acid (3 ml) was stirred at 90° C. for 7 hours. The cooled mixture was then carefully quenched by the addition of water (25 ml), and the mixture was extracted with dichloromethane (3×30 ml). The combined organic extracts were washed with 2M sodium carbonate solution and brine (30ml), then dried (MgSO4) and concentrated under reduced pressure. The residual black gum was purified by distillation to afford the title compound, 330 mg. 1H-NMR (CDCl3, 400 MHz) δ: 0.82 (2×s, 6H), 1.02-1.20 (m, 4H), 1.35 (m, 3H), 1.50 (m, 2H), 1.78 (m, 2H), 3.40 (t, 2H).

후처리

  1. customThe cooled mixture was then carefully quenched by the addition of water (25 ml)
  2. extractionthe mixture was extracted with dichloromethane (3×30 ml)
  3. washThe combined organic extracts were washed with 2M sodium carbonate solution and brine (30ml)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated under reduced pressure
  6. distillationThe residual black gum was purified by distillation

출처 및 근거

ORD 기록
ord-b70b1eb391784f9eb183704d982e5635
출처 데이터셋
uspto-grants-2005_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06958402B2

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