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Potassium Carbonate → 1-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzene

HRID 1784830
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1784830
[Br:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[C:6]([I:8])[CH:7]=1.C(=O)([O-])[O-].[K+].[K+].[CH3:16][O:17][C:18]1[CH:25]=[CH:24][C:21]([CH2:22]Cl)=[CH:20][CH:19]=1>CN(C=O)C.C(OC)(C)(C)C.O.COC1C=CC(CCl)=CC=1>[Br:1][C:2]1[CH:3]=[C:4]([O:9][CH2:22][C:21]2[CH:24]=[CH:25][C:18]([O:17][CH3:16])=[CH:19][CH:20]=2)[CH:5]=[C:6]([I:8])[CH:7]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 3

HCID 11430Potassium CarbonateHCID 699934-Methyloxybenzyl chlorideHCID 226301823-Bromo-5-iodophenol

Produkt 1

HCID 509940261-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzeneAusbeute 77,8 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 699934-Methyloxybenzyl chlorideKatalysator
HCID 962
Water
Lösungsmittel
HCID 6228DimethylformamideLösungsmittel
HCID 15413tert-Butyl methyl etherLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

3-Bromo-5-iodo-phenol (8.48 g, 28.37 mmol) was dissolved in DMF (50 mL) under dry argon and cooled to 0° C. Then potassium carbonate (3.92 g, 28.37 mmol) was added, followed by drop wise addition of 4-methoxybenzyl chloride (3.7 mL, 27.0 mmol). The mixture was slowly warmed to room temperature and stirred for 20 h. Additional 4-methoxybenzyl chloride (0.19 mL, 1.4 mmol) was added and the mixture was stirred for additional 24 h at room temperature. The reaction mixture was diluted with tert-butylmethyl ether (300 mL) and water (150 mL). The layers were separated and the aqueous one extracted with tert-butylmethyl ether (2×150 mL). The combined organics were washed with water and brine (150 mL), dried (Na2SO4) and concentrated to give the crude product which was purified by flash chromatography on silica gel (330 g, AcOEt/heptane 1:9). 1-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzene (8.80 g, 59%, purity 80%, HPLC 220 nm) was obtained as a yellow oil.

Aufarbeitung

  1. temperatureThe mixture was slowly warmed to room temperature
  2. stirringthe mixture was stirred for additional 24 h at room temperature
  3. customThe layers were separated
  4. extractionthe aqueous one extracted with tert-butylmethyl ether (2×150 mL)
  5. washThe combined organics were washed with water and brine (150 mL)
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated
  8. customto give the crude product which
  9. customwas purified by flash chromatography on silica gel (330 g, AcOEt/heptane 1:9)

Quellen und Nachweise

ORD-Eintrag
ord-c5c30b34a447446bb1f71cc9561ce8c5
Quelldatensatz
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07504401B2

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