HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432593Generated: October 27, 2026
Ethyl bromoacetate → HCID 24823447, compound
https://huagongshe.com/reaction/432593
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 6-methoxy-3,4-dihydroisoquinolin-1(2H)-one | HCID 10607392 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 24823447 | HCID 24823447 | 91.7% |
Reaction Steps
To a solution of 3,4-dihydro-6-methoxy-1(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 hexamethyldisilazide (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06664250B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-647f5e717d4e45589042c33e201e766b |
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| Source note | uspto-grants-2003_12 |
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