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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206673Generated: October 31, 2026

4,7-Dibromo-N-methoxy-N-methyl-2,3-dihydro-1H-indene-5-carboxamide → (4,7-Dibromo-2,3-dihydro-1H-inden-5-yl)(4-ethylphenyl)methanone

https://huagongshe.com/reaction/2206673

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,7-Dibromo-N-methoxy-N-methyl-2,3-dihydro-1H-indene-5-carboxamideHCID 86714017—
ReactantHCID 178436501HCID 178436501—
SolventTetrahydrofuranHCID 8028—
Product(4,7-Dibromo-2,3-dihydro-1H-inden-5-yl)(4-ethylphenyl)methanoneHCID 7111053985%

Reaction Steps

To a solution of amide 9 (0.27 g, 0.73 mmol) in anhydrous THF (2.7 mL) was added dropwise 4-ethylphenylmagnesium bromide (3.65 mL of 0.5 M in THF, 1.83 mol) at 0° C. under nitrogen atmosphere. The mixture was warmed up to room temperature slowly and stirred at room temperature for 15 h. The reaction mixture was quenched with 1 M HCl solution (10 mL) and extracted with EtOAc (20 mL). The organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography to provide the compound 10 (0.25 g, 0.62 mmol, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371303B2
Source datasetuspto-grants-2016_06
ORD IDord-bd44af28324f438aa1b70c39927358cd
Source noteuspto-grants-2016_06