Bromine → 4-Bromo-2-fluoro-5-methylphenol

HRID 529413Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 529413
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[OH:9].[Br:10]Br>C(O)(=O)C>[Br:10][C:6]1[C:5]([CH3:8])=[CH:4][C:3]([OH:9])=[C:2]([F:1])[CH:7]=1

Komponenten

4

Edukt 2

HCID 24408BromineHCID 182387Phenol, 2-fluoro-5-methyl-

Produkt 1

HCID 108997434-Bromo-2-fluoro-5-methylphenolAusbeute 98 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

2-fluoro-5-methylphenol (23.8 g, 0.19 mol) and bromine (9.7 ml, 0.19 mol) are combined in 50 ml of glacial acetic acid and stirred at RT for one hour. Acetic acid was removed under vacuum. The liquid was diluted with ethyl acetate and washed with water. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated to afford 4-bromo-2-fluoro-5-methylphenol (38 g, 98% yield) as a colorless liquid. No [M+H] peak by LCMS. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.98 (s, 1 H) 2.22 (s, 3 H) 6.81 (dd, J=9.15, 0.54 Hz, 1 H) 7.17 (d, J=9.88 Hz, 1 H)

Aufarbeitung

  1. customAcetic acid was removed under vacuum
  2. additionThe liquid was diluted with ethyl acetate
  3. washwashed with water
  4. washThe organic layer was washed with brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-a4a633c0697c46dcbd7b40cb51905e59
Quelldatensatz
uspto-grants-2016_05
Patentnummer
US09346827B2

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