HuagongsheHuagongshe Chemistry Print Report · For research reference only
5H-Inden-5-one, 7-butyl-1,2,3,6,7,7a-hexahydro- → 5H-Inden-5-one, 7-butyloctahydro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5H-Inden-5-one, 7-butyl-1,2,3,6,7,7a-hexahydro- | HCID 20559859 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5H-Inden-5-one, 7-butyloctahydro- | HCID 21156060 | 94% |
Reaction Steps
5-Butylbicyclo [4.3.0] non-1-en-3-one (120 g) is hydrogenated in ethyl acetate (125 ml) over 1.5 g of 5% palladium on carbon at a pressure of 4 atmospheres in a Parr apparatus. The solution is filtered through celite to remove the catalyst, concentrated, and the residue is vacuum distilled through a 12" Vigreaux column to yield 114 g (bp 98°-102° C. at 0.5 mm) of 5-butylbicyclo [4.3.0] nonan-3-one represented by the structure: ##STR10##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04206089 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-306edd546c4d49ec8a9a8202f22266ad |
| Source note | uspto-grants-1980_06 |