HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648792Generated: October 29, 2026
1,2-Dibromoethane → HCID 14150219, compound
https://huagongshe.com/reaction/648792
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 20145882 | HCID 20145882 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14150219 | HCID 14150219 | 47% |
Reaction Steps
In a manner similar to the procedure described in Example B except that a 100 milliliter three-necked Morton flask was used, 10.0 grams (43.0 mmol) of ethyl 3-[(4-cyanophenyl)amino]-3-oxopropanoate, 14.8 grams (108.0 mmol) of anhydrous potassium carbonate, 40 milliliters of anhydrous dimethylformamide and 3.7 milliliters (43.0 mmol) of 1,2-dibromoethane were reacted for a period of 8 days to give 5.19 grams (20.0 mmol) of ethyl 1-(4-cyanophenylaminocarbonyl)cyclopropanecarboxylate as a colorless solid having a melting point of 132.0° C.-133.5° C. The total yield was 47 percent. An analytical sample was prepared by recrystallization from hexane-ethyl acetate having a melting point of 133.0° C.-134.0° C. NMR analysis of the product indicated the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04736056 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-1a5691dfceda44549b1689cb1589d07f |
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| Source note | uspto-grants-1988_04 |
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