HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloroacetyl chloride → 7,7-Dichloro-4-heptylbicyclo[3.2.0]heptan-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloroacetyl chloride | HCID 6420 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 13924057 | HCID 13924057 | — |
| Reactant | 3-Heptylcyclopentene | HCID 13924079 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Zinc copper couple | HCID 10290809 | — |
| Product | 7,7-Dichloro-4-heptylbicyclo[3.2.0]heptan-6-one | HCID 13924067 | — |
Reaction Steps
The next procedure followed is that of the preceding Example for the preparation of 7,7-dichloro-4-(5-ethoxyheptyl)bicyclo [3.2.0] heptan-6-one, substituting 3-heptylcyclopentene (49 g, 0.30 moles) diluted in ether (490 ml), trichloroacetyl chloride (97 g, 0.53 moles) and phosphorous oxychloride (81 g, 0.53 moles) both diluted with ether (150 ml), zinc/copper couple (30 g, 0.59 moles) were used. The crude product is submitted to short path distillation and subsequently fractionally distilled under reduced pressure, leaving a clear, colorless oil of 7,7-dichloro-4-heptylbicyclo[3.2.0]heptan-6-one (20.6 g, 0.075 moles), BP 115° C./0.22 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04731458 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-b469a3b2863f4883ba8931831bcf820d |
| Source note | uspto-grants-1988_03 |