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

HRID 51307
ノート
印刷プレビュー

反応式

HRID 51307 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

反応条件

温度
90 °C

実験手順

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 (30 ml), 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).

後処理

  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 (30 ml)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated under reduced pressure
  6. distillationThe residual black gum was purified by distillation

出典と根拠

ORDレコード
ord-0ddef5f78e7e4f848ae734dcd107fa9d
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06713496B2

反応ノート

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