Phenol → 2-Nitro-5-phenoxytoluene

HRID 862669

Reaction equation

HRID 862669 reaction equation
[C:1]1([OH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(=O)([O-])[O-].[K+].[K+].F[C:15]1[CH:16]=[CH:17][C:18]([N+:22]([O-:24])=[O:23])=[C:19]([CH3:21])[CH:20]=1>CN(C)C(=O)C>[N+:22]([C:18]1[CH:17]=[CH:16][C:15]([O:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[CH:20][C:19]=1[CH3:21])([O-:24])=[O:23]

Participants

5

Conditions

Temperature
20 °C

Procedure

14.1 g (150 mmol) of phenol were dissolved in 120 ml of anhydrous N,N-dimethylacetamide, while stirring, 20.6 g (150 mmol) of finely powdered potassium carbonate were added and the mixture was stirred at 70°-80° C. for 30 minutes. After cooling to 20° C., 23.25 g (18.3 ml, 150 mmol) of 5-fluoro-2-nitrotoluene were added dropwise, the mixture was heated at 135°-140° C. for 2 hours and, after cooling, concentrated in vacuo, the residue was introduced into ice and the crystalline product was filtered off with suction, washed with water and dried, 30 g, melting point 43°-46° C.

Workup

  1. stirringthe mixture was stirred at 70°-80° C. for 30 minutes
  2. temperaturethe mixture was heated at 135°-140° C. for 2 hours
  3. temperatureafter cooling
  4. concentrationconcentrated in vacuo
  5. additionthe residue was introduced into ice
  6. filtrationthe crystalline product was filtered off with suction
  7. washwashed with water
  8. customdried

Sources & evidence

ORD record
ord-defb0b4fd5514463b5bdb790daef7d08
Source dataset
uspto-grants-1998_02
Patent number
US05719164

Linked notes

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