Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Anthranilamide | HCID 6942 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13566148 | HCID 13566148 | 23.3% |
Reaction Steps
To 2 g of ortho-aminobenzamide were added 4.04 g (2 equivalents) of potassium carbonate, 4.94 g (2 equivalents) of ethyl bromoacetate, and the mixture was stirred under heating at 160° C. for 3 hours. After cooling to room temperature, water was added and the mixture extracted with ethyl acetate. After washing with aqueous sodium chloride, the mixture was dried over anhydrous magnesium sulfate, followed by evaporation of the solvent. The residue was developed with hexaneethyl acetate (1:2) by silica gel column chromatography to obtain 760 mg of the desired compound (yield 23.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05312625 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-6859c112e49c426abcd69d49d00b04ea |
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| Source note | uspto-grants-1994_05 |
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