HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Ethyl2-(1,2-dihydro-1-acenaphthylenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl2-(1,2-dihydro-1-acenaphthylenylidene)acetate | HCID 70179131 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl2-(1,2-dihydro-1-acenaphthylenyl)acetate | HCID 13715672 | — |
Reaction Steps
55 mg of PdCl2 in 5 ml of methanol are treated with 25 mg of sodium borohydride. After 15 minutes' stirring, the compound obtained in Step B (1 g, 4.20.10−3 mol), diluted with methanol (25 ml), is added. The mixture is purged with argon and placed under a hydrogen atmosphere. After 2 hours 30 minutes' hydrogenation, the reaction mixture is filtered over Celite, rinsed and then evaporated under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06423870B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-455c973d4abd4c9dbc62bc0345c0c13c |
| Source note | uspto-grants-2002_07 |