Hydrochloric Acid → 3,3'-Difluorobenzophenone oxime

HRID 1058795Notes

Reaction equation

HRID 1058795 reaction equation
Cl.[NH2:2][OH:3].[F:4][C:5]1[CH:6]=[C:7]([CH:17]=[CH:18][CH:19]=1)[C:8]([C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=1)=O.[OH-].[Na+].Cl>O.C(O)C>[F:4][C:5]1[CH:6]=[C:7]([CH:17]=[CH:18][CH:19]=1)[C:8](=[N:2][OH:3])[C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=1

Participants

7

Conditions

Temperature
20 °C

Procedure

3-3′-Difluorobenzophenone oxime may be prepared according to the following procedure: a solution of 1.6 g of hydroxylamine hydrochloride in 8 cm3 of water is poured dropwise into a solution of 5.0 g of 3,3′-difluorobenzophenone in 10 cm3 of ethanol, and then 1.2 g of sodium hydroxide pellets are added in small fractions. The reaction mixture, heated under reflux for 10 minutes, is cooled to 20° C. and then acidified with 7.5 cm3 of 4 N hydrochloric acid. Once triturated, the oily precipitate obtained becomes a white solid which is filtered, washed with water and then dried at 35° C. under reduced pressure (2.7 kPa). 5.17 g of 3,3′-difluorobenzophenone oxime are obtained in the form of a white solid.

Workup

  1. temperatureThe reaction mixture, heated
  2. temperatureunder reflux for 10 minutes
  3. customOnce triturated
  4. customthe oily precipitate obtained
  5. filtrationis filtered
  6. washwashed with water
  7. customdried at 35° C. under reduced pressure (2.7 kPa)

Sources & evidence

ORD record
ord-b102b1a337004c1db555fae63c10bd5b
Source dataset
uspto-grants-2003_02
Patent number
US06518264B2

Reaction notes

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