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Potassium Carbonate → (2-Ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfide

HRID 25280
Notes
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Reaction equation

HRID 25280 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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 11430Potassium CarbonateHCID 677091,1,1-Trifluoro-2-iodoethaneHCID 221708901,1'-Thiodi-[2-ethoxymethoxy-5-(4-trifluoromethylphenyl)benzene]HCID 23689980Sodium Formaldehyde Sulfoxylate

Product 1

HCID 86587598(2-Ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfideYield 151.1%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent

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

  1. customThe resulting reaction mixture
  2. extractionextracted with 50 ml of ethyl acetate twice
  3. washThe ethyl acetate layer was washed with 50 ml of water twice
  4. dry with materialdried over anhydrous magnesium sulfate
  5. distillationthe ethyl acetate was distilled off under reduced pressure
  6. customPurification of the residue by silica gel column chromatography

Sources & evidence

ORD record
ord-c3157614ddee40f7b889ddcb92241301
Source dataset
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06858639B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes