Thionyl Chloride → HCID 13330038, compound
Reaction equation
[F:1][C:2]([F:13])([F:12])[C:3]([NH:5][C:6]([CH3:11])([CH3:10])[C:7](O)=[O:8])=[O:4].S(Cl)([Cl:16])=O>>[F:1][C:2]([F:13])([F:12])[C:3]([NH:5][C:6]([CH3:11])([CH3:10])[C:7]([Cl:16])=[O:8])=[O:4]Participants
3
Procedure
0.54 g (2.71 mmol) 2-trifluoroacetylamino-isobutyric acid are combined with 1.8 ml (2.47 g, 20.8 mmol) thionyl chloride and refluxed for 2 hours with stirring. The mixture is then evaporated down i. vac. and any remaining thionyl chloride is eliminating by blowing dry nitrogen over it. The residue is taken up in diethyl ether and petroleum ether and evaporated down again by blowing dry nitrogen over it.
Workup
- temperaturerefluxed for 2 hours
- customThe mixture is then evaporated down i
- custompetroleum ether and evaporated down again
Sources & evidence
- ORD record
- ord-cd764f8397504778a8183c1ed5e2f6a4
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07476663B2
Reaction notes
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