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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591356Generated: October 23, 2026

Ethyl Acetate → 2,2'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthalene

https://huagongshe.com/en/reaction/1591356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2,2'-Dibromo-1,1'-binaphthylHCID 619909—
ReactantHCID 178418361HCID 178418361—
CatalystRutheniumHCID 23950—
SolventEthanolHCID 702—
Product2,2'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthaleneHCID 1494277785.7%

Reaction Conditions

Temperature30 °C

Reaction Steps

Into a 500-ml stainless steel-made autoclave were introduced 35 g (0.085 mole) of 2,2'-dibromo-1,1'-binaphthyl (III), 5.25 g of 5%-ruthenium-on=carbon (manufactured by NECHEM CAT Inc.), 130 ml of ethyl acetate, and 130 ml of 95% ethanol. Hydrogenation was conducted at a hydrogen pressure of 50 kg/cm2 and a temperature of 100° C. for 20 hours, and it was then ascertained that the molar amount of hydrogen absorbed by the substrate had become four times that of the substrate. Thereafter, the reaction mixture was cooled to 30° C. and filtered to remove the catalyst. The resulting filtrate was allowed to stand at room temperature for a night, and crystals deposited were then collected by filtration. Thus, 30.6 g of the titled compound (IV) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206399
Source datasetuspto-grants-1993_04
ORD IDord-ebc3091b10114e6f9c5195ebe29ae605
Source noteuspto-grants-1993_04