HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164830Generated: November 1, 2026
Potassium Hydroxide → 4-chloro-6,7-dihydro-5H-dibenzo[a,c]cycloheptene
https://huagongshe.com/reaction/2164830
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 8-chloro-6,7-dihydro-5H-dibenzo[a,c]cycloheptene-5-one | HCID 20403345 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 4-chloro-6,7-dihydro-5H-dibenzo[a,c]cycloheptene | HCID 13281339 | — |
Reaction Steps
Under a dry nitrogen atmosphere a stirred mixture of 8-chloro-6,7-dihydro-5H-dibenzo[a,c]cycloheptene-5-one (2.6 grams, 0.011 mole), 85% hydrazine hydrate (5 ml, 0.1 mole), potassium hydroxide (4 grams, 0.071 mole) and ethylene glycol (30 ml) was heated at reflux for 1.5 hours. Sufficient volatiles were removed by distillation to increase the pot temperature to 200° while maintaining reflux. The two-phase reaction mixture was refluxed at that temperature for three hours. The mixture was cooled, poured into ice water, and the resultant mixture extracted with diethyl ether. The extract was washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was evaporated under reduced pressure to give a yellow oil. The oil was purified by distillation to give 4-chloro-6,7-dihydro-5H-dibenzo[a,c]cycloheptene (bp 119°-126°/0.15 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04507317 |
|---|
| Source dataset | uspto-grants-1985_03 |
|---|
| ORD ID | ord-c58b508672664ae9b5ad1d7c6a6f386c |
|---|
| Source note | uspto-grants-1985_03 |
|---|