Réaction #155391

ord-92c3430aed074b879487da802bcbe81f

Équation de réaction

c1c[nH]cn1
imidazole
Oc1ccc(O)cc1
hydroquinone
CC(C)(C)[Si](C)(C)Cl
tert-butyldimethylsilyl chloride
CC(C)(C)[Si](C)(C)Oc1ccc(O)cc1
4-(tert-butyldimethylsilyloxy)phenol

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionwas extracted with 2×50 mL of ether
  2. 2
    SéchageThe combined organic layer was dried over anhydrous Na2SO4
  3. 3
    Filtrationfiltered
  4. 4
    ConcentrationThe filtrate was concentrated under reduced pressure
  5. 5
    Autrepurified by column chromatography on silica gel with 5% ethyl acetate-hexanes

Mode opératoire

A solution of 2.9 parts of imidazole, 1.99 parts of hydroquinone and 3 parts of tert-butyldimethylsilyl chloride in 10 mL of dimethylformamide was stirred at room temperature for 1 hr 45 min. The reaction was monitored by TLC showed formation of product. The reaction mixture was diluted with 50 mL of deionized water and product was extracted with 2×50 mL of ether. The combined organic layer was dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated under reduced pressure and purified by column chromatography on silica gel with 5% ethyl acetate-hexanes to yield 2.24 parts 4-(tert-butyldimethylsilyloxy)phenol. NMR was used to confirm the following structure.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08822233B2uspto-grants-2014_09