Tetrahydrofuran → (5-Bromo-thiophen-2-yl)-p-tolyl-methanol

HRID 1891778Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1891778
[O:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[Br:6][C:7]1[S:8][C:9](Br)=[CH:10][CH:11]=1.[CH2:13]([Li])[CH2:14][CH2:15][CH3:16]>O>[Br:6][C:7]1[S:8][C:9]([CH:5]([C:4]2[CH:13]=[CH:14][C:15]([CH3:16])=[CH:2][CH:3]=2)[OH:1])=[CH:10][CH:11]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To an anhydrous tetrahydrofuran (70.0 mL) solution of 2,5-dibromothiophene (5.00 g, 19.6 mmol) was added dropwise n-butyl lithium (2.55 M n-hexane solution, 7.69 mL, 19.6 mmol) on a dry ice-ethanol bath (−78° C.) under nitrogen atmosphere, which was stirred for 20 minutes at −78° C. polaldehyde (2.35 g, 19.6 mmol) was then added dropwise and stirred for 10 minutes at −78° C. The reaction mixture was allowed to room temperature and water was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:5→1:1) to obtain the tile compound (4.30 g, 77.5%).

Aufarbeitung

  1. additionwas then added dropwise
  2. stirringstirred for 10 minutes at −78° C
  3. customwas allowed to room temperature
  4. extractionfollowed by extraction with ethyl acetate
  5. washThe organic layer was washed with saturated aqueous sodium chloride
  6. customthe solvent was evaporated under a reduced pressure
  7. customThe residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:5→1:1)

Quellen und Nachweise

ORD-Eintrag
ord-f6fb28c33fa1476f891924ef65c79bca
Quelldatensatz
uspto-grants-2013_08
Patentnummer
US08507530B2

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