1-(4-Fluorophenoxy)-3-nitrobenzene → 3-(4-Fluorophenoxy)aniline

HRID 1281301Notes

Reaction equation

HRID 1281301 reaction equation
[F:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:8]=[C:9]([N+:13]([O-])=O)[CH:10]=[CH:11][CH:12]=2)=[CH:4][CH:3]=1>C(O)C.[Pd]>[F:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:8]=[C:9]([CH:10]=[CH:11][CH:12]=2)[NH2:13])=[CH:4][CH:3]=1

Participants

4

Reactant 1

HCID 235060301-(4-Fluorophenoxy)-3-nitrobenzene

Product 1

HCID 235060153-(4-Fluorophenoxy)anilineYield 91.8%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

EX-634B) 3-(4-Fluorophenoxy)nitrobenzene (1.15 g, 4.93 mmol) from EX-634A was dissolved in ethanol (45 mL), and the solution was hydrogenated for 4 h in the presence of 5% palladium on charcoal. After the mixture was filtered through celite, the ethanol was removed in vacuo. The product was purified by flash column chromatography on silica gel eluting with ethyl acetate in hexane (1:10) to give 0.92 g (90%) of 3-(4-fluorophenoxy)aniline as a yellow oil, 99% pure by HPLC analysis. HRMS calcd. for C12H11FNO: 204.0824 [M+H]+, found: 204.0837.

Workup

  1. filtrationAfter the mixture was filtered through celite
  2. customthe ethanol was removed in vacuo
  3. customThe product was purified by flash column chromatography on silica gel eluting with ethyl acetate in hexane (1:10)

Sources & evidence

ORD record
ord-5e7514ef98f043a1b6e576ca134fea5b
Source dataset
uspto-grants-2002_09
Patent number
US06451823B1

Reaction notes

Loading…