Triethylamine → 2-(T-Butyldimethylsilyloxy)-4-bromoanisole

HRID 1515435Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1515435
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:9][CH3:10])=[C:6]([OH:8])[CH:7]=1.C(N(CC)CC)C.[Si:18](Cl)([C:21]([CH3:24])([CH3:23])[CH3:22])([CH3:20])[CH3:19]>C(Cl)Cl.CN(C)C1C=CN=CC=1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:9][CH3:10])=[C:6]([CH:7]=1)[O:8][Si:18]([C:21]([CH3:24])([CH3:23])[CH3:22])([CH3:20])[CH3:19]

Komponenten

6

Versuchsvorschrift

To a solution of 5-bromo-2-methoxy-phenol (3.5 g, 17.2 mmol) dissolved in methylene chloride (50 mL) are added triethylamine (2.08 g, 20.6 mmol) and 4-dimethylaminopyridine (0.15 g, 0.86 mmol). Then tert-butyldimethylsilyl chloride is added slowly and the reaction mixture is stirred at room temperature for 16 h. The reaction is quenched with 10% of citric acid, and then the organic layer is washed with saturated sodium bicarbonate solution, a saturated sodium chloride solution, dried with magnesium sulfate, and concentrated in vacuo. Purification by silica gel chromatography (15% ethyl acetate-hexane) provides 5.6 g (100%) of the title compound as a colorless oil. 1H NMR (CDCl3): δ 6.82 (m, 2H), 6.58 (d, J=9 Hz, 1H), 3.74 (s, 3H), 0.95 (s, 9H), 0.05 (s, 6H).

Aufarbeitung

  1. customThe reaction is quenched with 10% of citric acid
  2. washthe organic layer is washed with saturated sodium bicarbonate solution
  3. dry with materiala saturated sodium chloride solution, dried with magnesium sulfate
  4. concentrationconcentrated in vacuo
  5. customPurification by silica gel chromatography (15% ethyl acetate-hexane)

Quellen und Nachweise

ORD-Eintrag
ord-7402ff6a063a47c7849dd24c2d3f8809
Quelldatensatz
uspto-grants-2012_07
Patentnummer
US08222424B2

Notizen zur Reaktion

Wird geladen…