Acetonitrile → 2,2,2-Trifluoro-N-(4-methoxyphenyl)acetimidoyl Chloride
Reaction equation
[F:1][C:2]([F:15])([F:14])[C:3]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[CH:8][CH:7]=1)=O.P(Cl)(Cl)([Cl:18])=O.C(N(CC)CC)C.C(#N)C>C(OCC)(=O)C>[CH3:13][O:12][C:9]1[CH:10]=[CH:11][C:6]([N:5]=[C:3]([Cl:18])[C:2]([F:15])([F:14])[F:1])=[CH:7][CH:8]=1Participants
6
Conditions
- Temperature
- 82 °C
Procedure
Five grams (22.8 mmol) of 2,2,2-trifluoro-N-(4-methoxyphenyl)acetamide, 7.02 g (45.6 mmol) of phosphorus oxychloride, 4.62 g (45.6 mmol) of triethylamine, and 25 ml of acetonitrile were introduced into a 100 ml flask and reacted for 22 hours while being refluxed (82° C.). After the reaction, the reaction solution was cooled to room temperature, 20 ml of ethyl acetate was added thereto, and the precipitate was then filtered off. The filtrate was subjected to solvent removal by evaporation, and the crude product thus obtained was purified by column chromatography (silica gel, ethyl acetate:hexane=3:7), resulting in 4.52 g of N-(4-methoxyphenyl)-2,2,2-trifluoroacetimidoyl chloride as a yellow liquid (yield: 83.4%).
Workup
- customreacted for 22 hours
- customAfter the reaction
- temperaturethe reaction solution was cooled to room temperature
- filtrationthe precipitate was then filtered off
- customThe filtrate was subjected to solvent removal by evaporation
- customthe crude product thus obtained
- customwas purified by column chromatography (silica gel, ethyl acetate:hexane=3:7)
Sources & evidence
- ORD record
- ord-a731e69042de41c38acd7fb8f18faa78
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07282609B2
Reaction notes
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