Benzoyl Peroxide → 4-Fluoro-3-methoxybenzyl bromide

HRID 1869453Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1869453
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[O:9][CH3:10].[Br:11]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[Br:11][CH2:8][C:5]1[CH:6]=[CH:7][C:2]([F:1])=[C:3]([O:9][CH3:10])[CH:4]=1

Komponenten

5

Edukt 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 27373722-Fluoro-5-methylanisole

Produkt 1

HCID 179892674-Fluoro-3-methoxybenzyl bromide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 5943Carbon TetrachlorideLösungsmittel

Versuchsvorschrift

41.7 g (297.54 mmol) of 2-fluoro-5-methylanisole is refluxed overnight with 59.9 g (327.48 mmol) of N-bromosuccinimide and 145 mg of benzoyl peroxide in 945 ml of carbon tetrachloride. The reaction mixture is filtered [through] a glass-fiber filter, and after the solvent is spun off, the residue (72.85 g>100%) is incorporated in crude form into the next stage.

Aufarbeitung

  1. filtrationThe reaction mixture is filtered [through] a glass-fiber
  2. filtrationfilter

Quellen und Nachweise

ORD-Eintrag
ord-ca382f91354c4014b22a7ac64dda1bbd
Quelldatensatz
uspto-grants-2009_12
Patentnummer
US07638515B2

Notizen zur Reaktion

Wird geladen…