4-Ethylaniline → HCID 10083997, compound

HRID 1087197Notes

Reaction equation

HRID 1087197 reaction equation
[F:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[CH:7][C:3]=1[C:4](Cl)=[O:5].[CH2:12]([C:14]1[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=1)[CH3:13]>[Cl-].[Zn+2].[Cl-].Cl>[NH2:18][C:17]1[CH:19]=[CH:20][C:14]([CH2:12][CH3:13])=[CH:15][C:16]=1[C:4]([C:3]1[CH:7]=[CH:8][C:9]([F:11])=[CH:10][C:2]=1[F:1])=[O:5]

Participants

5

Conditions

Temperature
200 °C

Procedure

Zinc chloride (7.2 g) was added portionwise to a stirred mixture of 2,4-difluorobenzoyl chloride (17 g) and 4-ethylaniline (5.3 g) at 180° C. The mixture was stirred for 2.5 hours at 200° C. and cooled to 120° C. To the mixture was added 3N hydrochloric acid (50 ml) and the resulting mixture was refluxed for 1.5 hours, then the supernatant was decanted out. The above procedure was repeated three times. 75% Sulfuric acid (40 ml) was added and the reaction mixture was stirred and heated at 140° C. for 2 hours. The reaction mixture was poured into ice (500 ml) and extracted with dichloromethane. The organic layer was washed with 3N hydrochloric acid (200 ml), 3N sodium hydroxide (200 ml) and water, dried, and evaporated. The oily residue (5.7 g) was purified by column chromatography on silica gel (170 g) eluting with toluene to give crystals of 2-amino-5-ethyl-2',4'-difluorobenzophenone (3.5 g).

Workup

  1. temperaturecooled to 120° C
  2. temperaturethe resulting mixture was refluxed for 1.5 hours
  3. customthe supernatant was decanted out
  4. addition75% Sulfuric acid (40 ml) was added
  5. stirringthe reaction mixture was stirred
  6. temperatureheated at 140° C. for 2 hours
  7. additionThe reaction mixture was poured into ice (500 ml)
  8. extractionextracted with dichloromethane
  9. washThe organic layer was washed with 3N hydrochloric acid (200 ml), 3N sodium hydroxide (200 ml) and water
  10. customdried
  11. customevaporated
  12. customThe oily residue (5.7 g) was purified by column chromatography on silica gel (170 g)
  13. washeluting with toluene

Sources & evidence

ORD record
ord-0ec2cb67f84642eb8471fb3ababba179
Source dataset
uspto-grants-1991_07
Patent number
US05034417

Reaction notes

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