HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → HCID 14150221, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(2,4-Dichlorophenyl)-3-ethoxy-3-oxopropanimidic acid | HCID 12741175 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14150221 | HCID 14150221 | 83.6% |
Reaction Steps
In a manner similar to the procedure described in Example B except that a one liter three-necked Morton flask was used, 39.0 grams (0.14 mol) of ethyl 3-[(2,4-dichlorophenyl)amino]-3-oxopropanoate, 53.9 grams (0.39 mol) of anhydrous potassium carbonate, 125 milliliters of anhydrous dimethylformamide and 13.4 milliliters (0.16 mol) of 1,2-dibromoethane were reacted for a period of 65 hours to give 35.3 grams (0.117 mol) of ethyl 1-(2,4-dichlorophenylaminocarbonyl)cyclopropanecarboxylate as a pale yellow solid having a melting point of 95.0° C.-96.0° C. The total yield was 83 percent. NMR analysis of the product indicated the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04736056 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-5f29f9f5c036478298e674657789e0f1 |
| Source note | uspto-grants-1988_04 |