Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | HCID 22170959 | HCID 22170959 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 117899706 | HCID 117899706 | 89.2% |
Reaction Steps
To 300 ml of toluene were added 32.0 g (119 mmol) of 2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl boronic acid produced by the method described in PCT International Publication No. WO 2007/034755 and 15.4 g (131 mmol) of N-methylmorpholine-N-oxide, followed by refluxing for 1 hour under heating. The reaction mixture was allowed to cool to room temperature. The solvent was distilled off under reduced pressure. The residue was subjected to extraction with ethyl acetate. The organic phase obtained was washed with water and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=4:1), to obtain 25.5 g (yield: 89%) of an intended product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09332754B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-df32cfdc2c794093b8d1ba1edb63a8e8 |
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| Source note | uspto-grants-2016_05 |
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