1,3,5-Trichlorobenzene → Ammonia

反応式

[F:1][C:2]1[CH:3]=[C:4]([CH:6]=[C:7]([F:9])[CH:8]=1)[NH2:5].ClC1C=C(Cl)C=C(Cl)C=1.[F:19][C:20]1[CH:25]=[C:24]([F:26])[CH:23]=[C:22]([F:27])[CH:21]=1>>[F:19][C:20]1[CH:25]=[C:24]([F:26])[CH:23]=[C:22]([F:27])[CH:21]=1.[NH3:5].[F:1][C:2]1[CH:3]=[C:4]([CH:6]=[C:7]([F:9])[CH:8]=1)[NH2:5]

参加物

反応物 3

HCID 79501,3,5-Trichlorobenzene

HCID 97451,3,5-Trifluorobenzene

HCID 965953,5-Difluoroaniline

生成物 3

HCID 222Ammonia

HCID 97451,3,5-Trifluorobenzene

HCID 965953,5-Difluoroaniline

実験手順

One embodiment of the present invention relates to the discovery that 3,5-difluoroaniline can be synthesized at high yields and high purity by fluorinating 1,3,5-trichlorobenzene in the presence of a polar solvent to make an intermediate 1,3,5-trifluorobenzene, and then aminating the 1,3,5-trifluorobenzene in the presence of aqueous or anhydrous ammonia to obtain the desired 3,5-difluoroaniline.