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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170739Generated: October 29, 2026

Methyl 4-(bromomethyl)benzoate → HCID 117665501, compound

https://huagongshe.com/reaction/2170739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(bromomethyl)benzoateHCID 256687—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 105541411HCID 105541411—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117665501HCID 11766550113.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of lithium diisopropylamide (2.0 M in THF, 0.50 mL, 1.0 mmol) was added to a solution of 4-(naphthalen-1-yl)-2,3-dihydro-1H-inden-1-one (254 mg, 0.98 mmol) in THF (3.4 mL) at −78° C. After 1 h at −78° C., a solution of methyl 4-(bromomethyl)benzoate (230 mg, 1.0 mmol) in THF (1.7 mL) was added via cannula. After 1 h at −78° C., the mixture was allowed to slowly warm to 0° C. After 30 min at 0° C., the reaction was quenched with saturated aqueous NH4Cl (25 mL), diluted with water (10 mL) and extracted with EtOAc (3×50 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated. The resulting crude residue was purified by combiflash (40 g column, hexanes→30% EtOAc/hexanes, gradient) to afford 53 mg (13%) of methyl 4-((4-(naphthalen-1-yl)-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-ee00e14dea954f8987e3319db629ab39
Source noteuspto-grants-2015_06