HCID 54509558, compound → 4-{4-[2-Chloro-4-(trifluoromethyl)phenoxy]phenoxy}pent-1-en-3-one

HRID 647389Notes

Reaction equation

HRID 647389 reaction equation
[Cl:1][C:2]1[CH:23]=[C:22]([C:24]([F:27])([F:26])[F:25])[CH:21]=[CH:20][C:3]=1[O:4][C:5]1[CH:19]=[CH:18][C:8]([O:9][CH:10]([CH3:17])[C:11]([O:15]C)=[CH:12][CH2:13]O)=[CH:7][CH:6]=1>C(Cl)Cl>[Cl:1][C:2]1[CH:23]=[C:22]([C:24]([F:25])([F:27])[F:26])[CH:21]=[CH:20][C:3]=1[O:4][C:5]1[CH:19]=[CH:18][C:8]([O:9][CH:10]([CH3:17])[C:11](=[O:15])[CH:12]=[CH2:13])=[CH:7][CH:6]=1

Participants

3

Reactant 1

HCID 54509558HCID 54509558, compound

Product 1

HCID 202524304-{4-[2-Chloro-4-(trifluoromethyl)phenoxy]phenoxy}pent-1-en-3-one

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

The foregoing alcohol (380 mg) is reacted with 35% HClO4 (4 ml) in CH2Cl2 (4 ml) at RT for 24 hours. The mixture is then extracted with CH2Cl2 and the combined extracts washed, dried and concentrated to dryness. The product is purified by prep. thin layer chromatography to give 4-[4-(2-chloro-4trifluoromethylphenoxy)phenoxy]-3-oxo-1-pentene, MS m/e 396 (M+).

Workup

  1. extractionThe mixture is then extracted with CH2Cl2
  2. washthe combined extracts washed
  3. customdried
  4. concentrationconcentrated to dryness
  5. customThe product is purified by prep

Sources & evidence

ORD record
ord-191d4d65faa440fd9284e7e4be275170
Source dataset
uspto-grants-1983_10
Patent number
US04408076

Reaction notes

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