HCID 86735506, compound → HCID 86735505, compound

HRID 1856450Notes

Reaction equation

HRID 1856450 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:14]([F:17])([F:16])[F:15])[CH:5]=[C:4]([N+:18]([O-])=O)[C:3]=1[O:21][C:22]1[C:27]([N+:28]([O-])=O)=[CH:26][C:25]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=2[C:37]([F:40])([F:39])[F:38])=[CH:24][C:23]=1[Cl:41].[H][H]>C(O)C.O=[Pt]=O>[NH2:18][C:4]1[CH:5]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:14]([F:16])([F:17])[F:15])[CH:7]=[C:2]([Cl:1])[C:3]=1[O:21][C:22]1[C:23]([Cl:41])=[CH:24][C:25]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=2[C:37]([F:40])([F:39])[F:38])=[CH:26][C:27]=1[NH2:28]

Participants

5

Procedure

A solution of 2-chloro-α,α,α-trifluoro-6-nitro-p-tolylphenyl ether (150 g., 0.472 mole) in ethanol (1200 ml.) was shaken in an atmosphere of hydrogen in a Parr apparatus in the presence of PtO2 (600 mg.) until uptake ceased. The catalyst was filtered off, the solvent removed, and the residue taken up in pentane (600 ml.) and filtered through activated silica gel (~15 g.) and the solvent removed. The residue was recrystallized from pentane at -20° C. to give 2-amino-6-chloro-α,α,α-trifluoro-p-tolylphenyl ether (94.1 g., 70%) m.p. 47°-53° C.

Workup

  1. filtrationThe catalyst was filtered off
  2. customthe solvent removed
  3. filtrationfiltered through activated silica gel (~15 g.)
  4. customthe solvent removed
  5. customThe residue was recrystallized from pentane at -20° C.

Sources & evidence

ORD record
ord-f80f7008bf04463da22cab29275a47fc
Source dataset
uspto-grants-1980_08
Patent number
US04219352

Reaction notes

Loading…