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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384961Generated: November 3, 2026

Ethyl bromoacetate → HCID 24823447, compound

https://huagongshe.com/reaction/1384961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant6-methoxy-3,4-dihydroisoquinolin-1(2H)-oneHCID 10607392—
SolventTetrahydrofuranHCID 8028—
ProductHCID 24823447HCID 2482344791.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3,4-dihydro-6-methoxy-l(2H)-isoquinolinone (852 mg, 4.81 mmol, prepared according to J. Chem. Soc., 1969, p 183) in THF (45 mL) at −78° C. was added 0.5M potassium hexamethyidisilazide (10.6 mL, 5.28 mmol) dropwise and the reaction mixture stirred at −78° C. for 5 minutes. The reaction mixture was warmed to 0° C. in a ice/water bath and ethyl bromoacetate (1.20 g, 7.21 mmol) was added dropwise and the mixture stirred at that temperature for 1 hour, and then at room temperature for 2 hours. The reaction mixture was quenched by addition of sat. NaHCO3, diluted with ethyl acetate, and the organic layer was washed with saturated NaHCO3 and then brine. It was dried (MgSO4) and concentrated in vacuo to afford the title compound (1.1 g, 86%) as a yellow solid. Molecular weight (MS): 263.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262068B1
Source datasetuspto-grants-2001_07
ORD IDord-3aa49c09af9844c29967e88abaa7a1d9
Source noteuspto-grants-2001_07