Reaction equation
[S:1]([C:23]1[CH:28]=[C:27]([C:29]2[CH:34]=[CH:33][C:32]([C:35]([F:38])([F:37])[F:36])=[CH:31][CH:30]=2)[CH:26]=[CH:25][C:24]=1[O:39][CH2:40][O:41][CH2:42][CH3:43])C1C=C(C2C=CC(C(F)(F)F)=CC=2)C=CC=1OCOCC.C(S([O-])=O)O.[Na+].C(=O)([O-])[O-].[K+].[K+].[F:56][C:57]([F:61])([F:60])[CH2:58]I>CN(C)C=O.O>[F:56][C:57]([F:61])([F:60])[CH2:58][S:1][C:23]1[CH:28]=[C:27]([C:29]2[CH:34]=[CH:33][C:32]([C:35]([F:37])([F:36])[F:38])=[CH:31][CH:30]=2)[CH:26]=[CH:25][C:24]=1[O:39][CH2:40][O:41][CH2:42][CH3:43]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
3.3 g (5.0 mmol) of 1,1′-thiodi-[2-ethoxymethoxy-5-(4-trifluoromethylphenyl)benzene], 3.0 g (19.5 mmol) of Rongalite, 3.0 g (21.7 mmol) of potassium carbonate and 3.2 g (17.6 mmol) of 2,2,2-trifluoroethyl iodide were stirred in 50 ml of N,N-dimethylformamide at room temperature for 3 hours. The resulting reaction mixture was poured into 300 ml of water and extracted with 50 ml of ethyl acetate twice. The ethyl acetate layer was washed with 50 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 3.1 g of [2-ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfide (yield 75.6%) as a pale yellow viscous liquid (nD20 1.5213).
Workup
- customThe resulting reaction mixture
- extractionextracted with 50 ml of ethyl acetate twice
- washThe ethyl acetate layer was washed with 50 ml of water twice
- dry with materialdried over anhydrous magnesium sulfate
- distillationthe ethyl acetate was distilled off under reduced pressure
- customPurification of the residue by silica gel column chromatography
Sources & evidence
- ORD record
- ord-dbdc957797184312a7eb0f8e9262850a
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07767626B2
Linked notes
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