Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | (S)-1,2-Difluoro-3-(1-nitrohex-5-en-2-yl)benzene | HCID 86681331 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 86681332 | HCID 86681332 | 138.3% |
Reaction Steps
In a 250 mL round-bottomed flask was dissolved (S)-1,2-difluoro-3-(1-nitrohex-5-en-2-yl)-benzene (4.14 g, 17.2 mmol) in methanol (21 mL) under nitrogen. After cooling to 0° C., sodium methoxide (4.12 mL, 18.0 mmol) was added via syringe. After stirring at 0° C. for 30 min, the temperature was lowered to −60° C. Conc. sulfuric acid (2.93 mL, 54.9 mmol) in 21 mL methanol was added dropwise. The resulting milky mixture was stirred at −60 to −20° C. for 4 h. It was diluted with ethyl acetate and saturated ammonium chloride solution. The layers were separated. The aqueous layer was extracted with ethyl acetate (2×40 mL). The combined organic layers were washed with brine, dried, and concentrated to a give tan oil (4.8 g), which was dissolved in chloroform (124 mL) Water (31 mL) was added followed by slow addition of trifluoroacetic acid (31 mL). The mixture was stirred at rt overnight for 18 h. The layers were separated. The aqueous layer was extracted with methylene chloride. The combined organic layers were dried and concentrated to give a light yellow oil (5 g, 100%). This was directly carried onto next reaction immediately.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748429B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-de24a9419e4e461994706e497a961822 |
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| Source note | uspto-grants-2014_06 |
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