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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384373Generated: October 30, 2026

6-Bromo-1-ethylidene-indan → 6-Bromo-1-ethyl-indan

https://huagongshe.com/reaction/384373

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-1-ethylidene-indanHCID 68613364—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product6-Bromo-1-ethyl-indanHCID 5748383389.2%

Reaction Steps

6-Bromo-1-ethylidene-indan 41a (3.07 g, 13.7 mmol) was dissolved in 80 mL of ethyl acetate followed by addition of palladium on carbon (0.61 g) at room temperature. The mixture was hydrogenated for 5 hours in a hydrogenator under 3 atm. of hydrogen. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered to remove palladium on carbon and the filter cake was washed with ethyl acetate (10 mL×3). The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography to obtain the title compound 6-bromo-1-ethyl-indan 41b (2.75 g, 88.7%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-4bfee9bd64bd4d9a86b81aac224a4014
Source noteuspto-grants-2013_02