1-(2-Bromophenyl)ethan-1-ol → (1S)-1-(2-iodophenyl)ethanol

HRID 1351671

反応式

HRID 1351671 の反応式
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C@@H:8]([OH:10])[CH3:9].O.O.[I-:13].[Na+]>[Cu]I.CNCCNC.O1CCOCC1>[I:13][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C@@H:8]([OH:10])[CH3:9]

参加物

6

反応条件

温度
150 °C

実験手順

To each of three identical Emrys microwave reaction vessels was added (S)-1-(2-bromophenyl)ethanol (1.67 g, 8.3 mmol), CuI (189 mg, 1.0 mmol), 1,4-dioxane (12.4 ml), N,N′-dimethylethylenediamine (0.18 ml, 1.7 mmol) and sodium iodide dihydrate (3.1 g, 16.6 mmol). Each vessel was sealed and heated in an Emrys microwave reactor to 150° C. for 2 h. On cooling, the mixtures were combined and partitioned between water (20 ml) and EtOAc (20 ml). The organic phase was washed with brine (20 ml), dried (MgSO4), filtered, and concentrated in vacuo. The crude product was taken up in isohexane (50 ml) and the solution held at −15° C. for 16 h to afford (S)-1-(2-iodophenyl)ethanol as a white crystalline solid (4.95 g).

後処理

  1. customTo each of three identical Emrys microwave reaction vessels
  2. customEach vessel was sealed
  3. temperatureOn cooling
  4. custompartitioned between water (20 ml) and EtOAc (20 ml)
  5. washThe organic phase was washed with brine (20 ml)
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-753537b8cefe465291c457c56dfc875d
出典データセット
uspto-grants-2007_05
特許番号
US07217740B2

関連ノート

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