1,3-Dibromobenzene → 4-(3-Bromophenyl)-tetrahydro-2H-pyran-4-ol

HRID 2060761Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2060761
Br[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Br:8])[CH:3]=1.C([Li])CCC.CCCCCC.[O:20]1[CH:25]=[CH:24][C:23](=[O:26])[CH:22]=[CH:21]1>C1COCC1>[Br:8][C:4]1[CH:3]=[C:2]([C:23]2([OH:26])[CH2:24][CH2:25][O:20][CH2:21][CH2:22]2)[CH:7]=[CH:6][CH:5]=1

Komponenten

6

Versuchsvorschrift

To a stirred −78° C. solution of 1,3-dibromobenzene (19.71 g, 81.05 mmol) in THF (150 mL) is added 1.6 M butyl lithium in hexane (50.66 mL, 81.05 mmol) and the reaction is stirred 10 minutes. 4H-Pyran-4-one, tetrahydro- (5.41 g, 54.04 mmol) is added dropwise and the reaction is stirred at −78° C. for 2 h. The reaction is quenched by addition of saturated aqueous ammonium chloride (25 mL) and is then diluted with minimal water and extracted with EtOAc. The organic layer is dried over Na2SO4 and the solvent is removed under reduced pressure to afford a residue that is purified by silica gel chromatography eluting with a linear gradient of 5% to 100% EtOAc in hexanes to give the title compound (11.18 g, 76%). GC-MS (m/e): (79Br/81Br) 256, 258 (M−1).

Aufarbeitung

  1. stirringthe reaction is stirred at −78° C. for 2 h
  2. customThe reaction is quenched by addition of saturated aqueous ammonium chloride (25 mL)
  3. additionis then diluted with minimal water
  4. extractionextracted with EtOAc
  5. dry with materialThe organic layer is dried over Na2SO4
  6. customthe solvent is removed under reduced pressure
  7. customto afford a residue that
  8. customis purified by silica gel chromatography
  9. washeluting with a linear gradient of 5% to 100% EtOAc in hexanes

Quellen und Nachweise

ORD-Eintrag
ord-ccddfd7d55b64b2e9e7c17975147f7ed
Quelldatensatz
uspto-grants-2012_10
Patentnummer
US08278441B2

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