2-Phenylthiophene → 5-Bromo-2-trifluoromethylphenyl 5-phenyl-2-thienyl ketone

HRID 1625873Notes

Reaction equation

HRID 1625873 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:11]([F:14])([F:13])[F:12])=[C:6]([CH:10]=1)[C:7]([OH:9])=O.[C:15]1([C:21]2[S:22][CH:23]=[CH:24][CH:25]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[C:15]1([C:21]2[S:22][C:23]([C:7]([C:6]3[CH:10]=[C:2]([Br:1])[CH:3]=[CH:4][C:5]=3[C:11]([F:14])([F:13])[F:12])=[O:9])=[CH:24][CH:25]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Participants

3

Reactant 2

HCID 699992-PhenylthiopheneHCID 509981405-Bromo-2-trifluoromethylbenzoic acid

Product 1

HCID 666089255-Bromo-2-trifluoromethylphenyl 5-phenyl-2-thienyl ketone

Procedure

The above 5-bromo-2-trifluoromethylbenzoic acid and 2-phenylthiophene were treated in a manner similar to Reference Example 5-(1) to give 5-bromo-2-trifluoromethylphenyl 5-phenyl-2-thienyl ketone as pale yellow crystals. APCI-Mass m/Z 411/413 (M+H).

Sources & evidence

ORD record
ord-d53463445d1c46e593e05f52ac3719fa
Source dataset
uspto-grants-2014_07
Patent number
US08785403B2

Reaction notes

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