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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706009Generated: October 30, 2026

5H-Inden-5-one, 7-butyl-1,2,3,6,7,7a-hexahydro- → 5H-Inden-5-one, 7-butyloctahydro-

https://huagongshe.com/reaction/1706009

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5H-Inden-5-one, 7-butyl-1,2,3,6,7,7a-hexahydro-HCID 20559859—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product5H-Inden-5-one, 7-butyloctahydro-HCID 2115606094%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206089
Source datasetuspto-grants-1980_06
ORD IDord-306edd546c4d49ec8a9a8202f22266ad
Source noteuspto-grants-1980_06