HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibenzosuberol → 5H-Dibenzo(a,d)cycloheptene, 10,11-dihydro-5-chloro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibenzosuberol | HCID 14588 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5H-Dibenzo(a,d)cycloheptene, 10,11-dihydro-5-chloro- | HCID 14587 | — |
Reaction Steps
350 ml of thionyl chloride are added dropwise at a temperature of 30 to 40° to a solution of 201.5 g of crude 10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ol in 700 ml of dry benzene over a period of 40 minutes. Subsequently, the mixture is heated to boiling under reflux for an additional 1.5 hours and concentrated in vacuo. The residue is diluted 2 to 3 times with 300 ml of benzene each time and in each case again evaporated. There is obtained 5-chloro-10,11-dihydro-5H-dibenzo[a,d]cycloheptene as a beige crystalline mass of melting point 99-101° which is used in the next step without further purification. By recrystallization from carbon tetrachloride there is obtained material of melting point 104°-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04513002 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-87f5ca0bdb56446c92665a4bd57c673b |
| Source note | uspto-grants-1985_04 |