4-Fluorobenzamide → 4-Fluorothiobenzamide
Reaction equation
[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH2:8])=O)=[CH:4][CH:3]=1.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:20])=CC=1>C1C=CC=CC=1>[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH2:8])=[S:20])=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4-Fluorobenzamide (5.0 g, 35.9 mmol) in benzene (100 ml) is added Lawesson's reagent (7.27 g, 18.0 mmol) and the resulting solution is heated to reflux for 1 hour. The solution is cooled to room temperature, concentrated and water (150 ml) added. The mixture is heated to reflux for 3 hours, and cooled to room temperature. The precipitate is filtered and dried under vacuum to yield 4-fluorothiobenzamide as a yellow solid (4.1 g, 71%).
Workup
- temperaturethe resulting solution is heated
- temperatureto reflux for 1 hour
- concentrationconcentrated
- additionwater (150 ml) added
- temperatureThe mixture is heated
- temperatureto reflux for 3 hours
- temperaturecooled to room temperature
- filtrationThe precipitate is filtered
- customdried under vacuum
Sources & evidence
- ORD record
- ord-1af37469ddc645919710fc250be82378
- Source dataset
- uspto-grants-2001_08
- Patent number
- US06277873B1
Reaction notes
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