HuagongsheHuagongshe Chemistry Print Report · For research reference only
5H-Dibenzo[a,d]cyclohepten-5-one → HCID 15818605, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5H-Dibenzo[a,d]cyclohepten-5-one | HCID 16679 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15818605 | HCID 15818605 | 93.8% |
Reaction Steps
To 150 mmol of ethyl magnesium bromide in 150 ml of ether are added 10 g (48.5 mmol) of dibenzosuberenone in 250 ml of ether at 0° C. After 3 hours at about 10° C., the mixture is cooled in an ice bath and 40 ml of saturated aqueous ammonium chloride are added slowly. Extractions of the aqueous phase with ether affords 10.75 g of a yellow oily residue. Purification by flash chromatography yields 8.5 g (74%) of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05508280 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-d006935632f849e2bf6f4ff1754f110e |
| Source note | uspto-grants-1996_04 |