HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387644Generated: October 29, 2026
Water → 5-bromo-2-(2-methoxyethyl)-3,4-dihydroisoquinolin-1(2H)-one
https://huagongshe.com/reaction/387644
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-bromo-2-(2-hydroxyethyl)-3,4-dihydroisoquinolin-1(2H)-one | HCID 68473635 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-bromo-2-(2-methoxyethyl)-3,4-dihydroisoquinolin-1(2H)-one | HCID 21865471 | — |
Reaction Steps
0.39 g of 5-bromo-2-(2-hydroxyethyl)-3,4-dihydroisoquinolin-1(2H)-one is dissolved under an inert atmosphere in 3 cm3 of dimethylsulfoxide at a temperature close to 20° C. 105 mg of finely ground potassium hydroxide are added. The reaction mixture is stirred for 30 min at a temperature close to 20° C., then 0.108 cm3 of iodomethane is introduced. The stirring is continued for 20 h at a temperature close to 20° C. 30 cm3 of water and 30 cm3 of ethyl ether are added. After decanting, the organic phase is washed with 30 cm3 of a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and concentrated using a rotary evaporator under reduced pressure (5 kPa). 170 mg of 5-bromo-2-(2-methoxyethyl)-3,4-dihydroisoquinolin-1(2H)-one are obtained in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372864B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-756d84f986ff42e19c47b87ae9739399 |
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| Source note | uspto-grants-2013_02 |
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