HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → HCID 54460731, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | HCID 21415567 | HCID 21415567 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178527711 | HCID 178527711 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Product | HCID 54460731 | HCID 54460731 | — |
Reaction Steps
To a solution of 46 g of 9-(chlorocarbonylmethyl)-9,10-dihydro-9,10-ethano-anthracene in 200 ml of xylene are added 10 g of 10% palladium carbon which is contaminated with quinoline-sulphur. Then at 120° C hydrogen is passed in and after 7 hours the catalyst is filtered off and the reaction mixture evaporated in vacuo. The residue is dissolved in methylene chloride and the methylene chloride solution is extracted with sodium carbonate solution. The organic phase is isolated, dried and evaporated, to yield as residue the crude 9,10-dihydro-9,10-ethano-anthryl-acetaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04017542 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-907eded97e474a579ef7bfeec166da98 |
| Source note | uspto-grants-1977_04 |