HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → HCID 68872204, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Cyproheptadine | HCID 2913 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | HCID 68875465 | HCID 68875465 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 68872204 | HCID 68872204 | — |
Reaction Steps
The product from Step 3 (2.54 g crude) and cyanoacetic acid (0.88 g, 10.4 mmol) were dissolved in DMF (10 mL) and Et3N (3.6 mL) was added. To the solution was added EDC (2.2 g, 11.4 mmol), and the mixture was allowed to stir at rt for 2 days. The reactin mixture was poured into water and extracted with ethyl acetate. The separated organic layer was dried over MgSO4, filtered, and concentrated to give a dark oil. The oil was dissolved in AcOH (5 mL) and the solution was heated at 100° C. for 4 hours then cooled and concentrated in-vacuo to give the title compound as a dark foam that was taken on without further purification. MS (ES+) m/e 540 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547779B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-525188c6465448da8fdc69741a6f1dbf |
| Source note | uspto-grants-2009_06 |