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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170737Generated: October 30, 2026

1-Indanone, 4-bromo- → HCID 117665512, compound

https://huagongshe.com/reaction/2170737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Indanone, 4-bromo-HCID 98713—
ReactantMethyl 4-(bromomethyl)benzoateHCID 256687—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117665512HCID 1176655124.4%

Reaction Steps

A solution of lithium diisopropylamide (2.0 M in THF, 2.5 mL, 5.0 mmol) was added to a solution of 4-bromo-2,3-dihydro-1H-inden-1-one (4-bromo-1-indanone, 960 mg, 4.55 mmol) in THF (9.1 mL) at −78° C. After 1 h at −78° C., a solution of methyl 4-(bromomethyl)benzoate (1.25 g, 5.46 mmol) in THF (5 mL) was added via cannula. The reaction mixture was allowed to warm to room temperature naturally. After stirring at room temperature overnight, the reaction was quenched with saturated aqueous NH4Cl (50 mL) and extracted with EtOAc (3×100 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated. The resulting crude residue was purified by combiflash (330 g column, hexanes→30% EtOAc/hexanes, gradient) to afford 72 mg (4%) of methyl 4-((4-bromo-1-oxo-2,3-dihydro-1H-inden-2-yl)methyl)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051294B2
Source datasetuspto-grants-2015_06
ORD IDord-f98460ab604d41f8b0d0177e7774ddf8
Source noteuspto-grants-2015_06