Benzyl Bromide → 4-(Benzyloxy)-1,2-benzenediol

HRID 1614723Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1614723
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[OH:9].[H-].[Na+].B(OCC)(OCC)OCC.[CH2:22](Br)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>CN(C)C=O>[CH2:22]([O:8][C:5]1[CH:6]=[CH:7][C:2]([OH:1])=[C:3]([OH:9])[CH:4]=1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1

Komponenten

6

Versuchsvorschrift

1.37 g of 1,2,4-trihydroxy benzene and 30 ml of anhydrous dimethylformamide were mixed together under an inert gas atmosphere and then 0.984 g of sodium hydride in suspension at 53% in oil was added at 15°-20° C. The mixture was stirred for one hour and 1.906 ml of triethyl borate were added. The mixture was stirred for one hour, and 1.29 ml of benzyl bromide in solution in 20 ml of dimethylformamide were added over 2 hours. The mixture was stirred for 16 hours at ambient temperature and then was poured into a water-ice-N hydrochloric acid mixture. Extraction took place with ethyl acetate followed by evaporation to dryness. The residue was washed with petroleum ether, and chromatographed on silica eluting with a cyclohexane-ethyl acetate (6-4) mixture to obtain 1.36 g of the crystallized expected product (Yield: 58%).

Aufarbeitung

  1. stirringThe mixture was stirred for one hour
  2. stirringThe mixture was stirred for 16 hours at ambient temperature
  3. extractionExtraction
  4. customfollowed by evaporation to dryness
  5. washThe residue was washed with petroleum ether
  6. customchromatographed on silica eluting with a cyclohexane-ethyl acetate (6-4) mixture
  7. customto obtain 1.36 g of the

Quellen und Nachweise

ORD-Eintrag
ord-9fd5685655574b3aaa8630db1cb685b6
Quelldatensatz
uspto-grants-1993_03
Patentnummer
US05198571

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