Methylamine → HCID 11391445, compound
Reaction equation
[CH3:1][NH2:2].IC[CH2:5][CH2:6][CH:7]([S:17][CH:18](CCCI)[CH2:19][CH2:20][C:21]([F:27])([F:26])[C:22]([F:25])([F:24])[F:23])CCC(F)(F)C(F)(F)F>O1CCCC1>[CH3:1][NH:2][CH2:5][CH2:6][CH2:7][S:17][CH2:18][CH2:19][CH2:20][C:21]([F:27])([F:26])[C:22]([F:25])([F:24])[F:23]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
45 g of methylamine is condensed in a solution of 30.6 g of 3-iodopropyl-4,4,5,5,5-pentafluoro-pentylsulfide in 200 ml of absolute tetrahydrofuran at a bath temperature of −78° C., and it is stirred for 1.5 hours at room temperature as well as for 4 hours at 60° C. in a pressurized reactor. To open the reactor, it is allowed to cool overnight to room temperature and then to −78° C. Then, it is allowed to come to room temperature, excess methylamine is evaporated, it is diluted with ethyl acetate, washed neutral, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with dichloromethane/methanol. 15.7 g of N-methyl-[3-(4,4,5,5,5-pentafluoro-pentylthio)-propyl]-amine is obtained as an oil.
Workup
- temperatureto cool overnight to room temperature
- customto −78° C
- customto come to room temperature
- customexcess methylamine is evaporated
- additionit is diluted with ethyl acetate
- washwashed neutral
- customdried on sodium sulfate
- concentrationconcentrated by evaporation in a vacuum
- customchromatographed on silica gel with dichloromethane/methanol
Sources & evidence
- ORD record
- ord-3e853f8779bc418ab06249047782d7e3
- Source dataset
- uspto-grants-2004_08
- Patent number
- US06780855B2
Reaction notes
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