Fluorobenzene → 2-Chloro-5-(4-fluorobenzoyl)pyridine
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:8][C:9]1[CH:17]=[CH:16][C:12]([C:13](Cl)=[O:14])=[CH:11][N:10]=1>CC(=O)OCC>[Cl:8][C:9]1[CH:17]=[CH:16][C:12]([C:13](=[O:14])[C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)=[CH:11][N:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The fluorobenzene (150 ml, 1.60 mmol) and 6-chloronicotinoyl chloride (17.7 g, 100 mmol) were converted to product in a manner substantially analogous to Preparation 1 to yield 15.2 g. (66.1%). EA, MS(FD), NMR.
Workup
- customto yield 15.2 g
Sources & evidence
- ORD record
- ord-a66b77c5358044c3925eef8fdd2c6fe6
- Source dataset
- uspto-grants-2002_03
- Patent number
- US06358971B1
Reaction notes
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