HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6,7-dihydro-5H-dibenzo[a,c]-cyclohepten-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 6,7-dihydro-5H-dibenzo[a,c]cyclohepten-4-carbonitrile | HCID 13281340 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 6,7-dihydro-5H-dibenzo[a,c]-cyclohepten-4-carboxamide | HCID 13391278 | — |
Reaction Steps
Under a dry nitrogen atmosphere a stirred mixture of 6,7-dihydro-5H-dibenzo[a,c]cyclohepten-4-carbonitrile (1.0 gram, 0.0045 mole) in ethanol (20 ml) and 10% aqueous sodium hydroxide (20 ml) was heated at reflux for two days. The mixture was cooled and poured into dilute hydrochloric acid (150 ml). The resulting mixture was extracted with five 100 ml portions of methylene chloride and the extracts combined. The combined extracts were washed with two 100 ml portions of water, dried over anhydrous magnesium sulfate and filtered. The solvent was removed from the filtrate by distillation under reduced pressure to leave 6,7-dihydro-5H-dibenzo[a,c]cyclohepten-4-carboxamide as a white solid (1.1 grams, mp>250°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04493844 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-e790eb2ad45443c69121c62b64a4a8f2 |
| Source note | uspto-grants-1985_01 |