Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19777981 | HCID 19777981 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57667896 | HCID 57667896 | — |
Reaction Steps
To N,N-dimethylformamide 10 mL solution of methyl 4-(bromomethyl)-2-nitrobenzoate 1.0 g, were added potassium carbonate 1.0 g and benzenethiol 0.39 mL at room temperature, and it was stirred at same temperature for 7 hours. Ethyl acetate was added to the reaction mixture, insoluble matter was filtrated, and water was added to it. The organic layer was separated and collected,dried over anhydrous magnesium sulfate after sequential washing with saturated sodium hydrogen carbonate aqueous solution and saturated sodium chloride aqueous solution, the solvent was removed under reduced pressure. The obtained residue was refined by silica gel column chromatography [eluent; hexane:ethyl acetate=4:1] to give methyl 2-nitro-4-((phenylthio)methyl)benzoate 0.70 g of pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08327467B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-7c7297f694c14e48969307ab31e8c4ea |
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| Source note | uspto-grants-2012_12 |
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