HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-malonic acid | HCID 20187933 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylacetic acid | HCID 12669091 | — |
Reaction Steps
200 g of 10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-malonic acid are heated to 180° while stirring for 30 minutes. After cooling to 120°, the residue is treated with about 1 l of benzene and heated to boiling while stirring and under reflux until all crystallized-out material has again dissolved. Subsequently, the mixture is treated with 500 ml of hexane, cooled to about 10° while stirring and while cooling with ice, left to stand in the cold overnight and subsequently the crystal slurry obtained is removed by filtration under suction. After washing with petroleum ether and drying at 50° in a vacuum drying oven, there is obtained 10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-acetic acid as beige crystals of melting point 163°-165°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04513002 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-4116dd72bef144b99b6f40d7eb2e8dd9 |
| Source note | uspto-grants-1985_04 |