Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 3450994 | HCID 3450994 | — |
| Product | HCID 67305472 | HCID 67305472 | — |
Reaction Steps
34.5 g of N-(3-chloro-2-methylphenyl)-4-methylbenzenesulfonamide was dissolved in 232 mL of DMF, and 21.4 g of ethyl bromoacetate and 19.3 g of potassium carbonate were added thereto, followed by stirring at 100° C. for 1 hour. The reaction liquid was cooled to room temperature, and then water was added, followed by extraction with ethyl acetate. The organic layer was washed with brine, and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=80:20) to obtain 34.6 g of ethyl N-(3-chloro-2-methylphenyl)-N-[(4-methylphenyl)sulfonyl]glycine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07973078B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-5436fa672e284b229315c24a26f71c4a |
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| Source note | uspto-grants-2011_07 |
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