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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111643Generated: November 1, 2026

Ethyl bromoacetate → HCID 68918090, compound

https://huagongshe.com/reaction/2111643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantHCID 23084577HCID 23084577—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68918090HCID 6891809096.7%

Reaction Steps

To a solution of 5,6-dimethyl-2-(3-fluorophenyl)-3-hydroxyisoindolin-1-one (0.15 g, 0.55 mmol) in anhydrous tetrahydrofuran (5 ml) was added 60% sodium hydride (24 mg, 0.60 mmol), and stirred on ice for 10 minutes. Then, ethyl bromoacetate (67 ml, 0.60 mmol) was added thereto, and stirred at 25° C. overnight. The reaction solution was concentrated under reduced pressure, and water was added to the residue, followed by extracting with ethyl acetate. The extract was washed with saturated brine, dried, and concentrated under reduced pressure to give 0.19 g of 5,6-dimethyl-2-(3-fluorophenyl)-3-ethoxycarbonylmethyloxy-isoindolin-1-one [IUPAC name: ethyl 2-{[2-(3-fluorophenyl)-5,6-dimethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl]oxy}-acetate].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521451B2
Source datasetuspto-grants-2009_04
ORD IDord-21a3c04f25f3440c8049299f7aa5599a
Source noteuspto-grants-2009_04