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

HRID 2376986Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2376986
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]

Komponenten

6

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

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).

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-69de509636014e999f9b79851edd5e22
Quelldatensatz
uspto-grants-2008_12
Patentnummer
US07468393B2

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