3-Phenoxyaniline → Methyl 3-[[(3-phenoxyphenyl)amino]methyl]benzoate

HRID 50490

Reaktionsgleichung

Reaktionsgleichung von HRID 50490
Br[CH2:2][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][CH:12]=1)[C:6]([O:8][CH3:9])=[O:7].[O:13]([C:20]1[CH:21]=[C:22]([CH:24]=[CH:25][CH:26]=1)[NH2:23])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C1CCCCC1.O.C(Cl)Cl>[O:13]([C:20]1[CH:21]=[C:22]([NH:23][CH2:2][C:3]2[CH:4]=[C:5]([CH:10]=[CH:11][CH:12]=2)[C:6]([O:8][CH3:9])=[O:7])[CH:24]=[CH:25][CH:26]=1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1

Komponenten

6

Versuchsvorschrift

EX-612A) Methyl 3-(bromomethyl)benzoate (7.2 g, 0.031 mol) was added dropwise to a solution of 3-phenoxyaniline (20.5 g, 0.11 mol) in 160 mL of cyclohexane. The reaction mixture was refluxed overnight then cooled to room temperature and diluted with water and methylene chloride. The layers were separated, and the aqueous layer was extracted with methylene chloride. The combined organic layers were washed with brine, dried over Na2SO4, and concentrated in vacuo to give a dark oil. The crude product was purified by reverse phase HPLC eluting with 20% to 90% acetonitrile in water to afford 6.2 g (59%) of the desired methyl 3-[[(3-phenoxyphenyl)amino]methyl]benzoate product as a yellow oil. ESMS m/z=334 [M+H]+.

Aufarbeitung

  1. temperatureThe reaction mixture was refluxed overnight
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with methylene chloride
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo
  7. customto give a dark oil
  8. customThe crude product was purified by reverse phase HPLC
  9. washeluting with 20% to 90% acetonitrile in water

Quellen und Nachweise

ORD-Eintrag
ord-7be87054bbfb41eca817d15373a0a048
Quelldatensatz
uspto-grants-2004_03
Patentnummer
US06710089B2

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