HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1,4-Ethanonaphthalen-2(1H)-one, 3,4-dihydro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1,4-Ethanonaphthalen-2-ol, 1,2,3,4-tetrahydro-, exo- | HCID 582616 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,4-Ethanonaphthalen-2(1H)-one, 3,4-dihydro- | HCID 582596 | 88.5% |
Reaction Steps
To a solution of 5.6 g of tricyclo[6.2.2.02,7]dodeca-2,4,6-trien-9-ol in 30 mL of DCM were added 110 mL of a 15% DMP solution in DCM. After stirring overnight 300 mL of EtOAc/Hept (1:1) were added, the obtained suspension was filtered over a pad of celite and the filtrated was concentrated in vacuo. The residue was treated again with EtOAc/Hept (1:1) and filtered over celite. This procedure was repeated twice to obtain 4.9 g of the desired compound as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08314253B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-327b7c94f4314aa39944ec100ec8d2af |
| Source note | uspto-grants-2012_11 |