HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597772Generated: October 25, 2026
Hydrochloric Acid → Isoquinolyl 4-methoxyphenyl ketone
https://huagongshe.com/reaction/597772
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Bromoanisole | HCID 7730 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Isoquinolinecarbonitrile | HCID 306057 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Isoquinolyl 4-methoxyphenyl ketone | HCID 693112 | — |
Reaction Steps
4-Bromoanisol (15.3 ml, 122 mmol) and a catalytic amount of 1,2-dibromoethane as an initiator were added to a mixed solution of magnesium (3059 mg, 125.8 mmol) and tetrahydrofuran (20 ml) under nitrogen atmosphere, and this reaction mixture was stirred while heating under reflux for 45 minutes. The mixture was cooled to 0° C., a solution of 1-isoquinolinecarbonitrile (10.78 g, 69.9 mmol) in tetrahydrofuran (30 ml) was added dropwise thereto, and this reaction mixture was stirred at room temperature for 2 hours. The reaction mixture was cooled on ice, concentrated hydrochloric acid (24 ml) and methanol (120 ml) were added, and this mixture was heated under reflux for 1.5 hours. After cooling on ice, the mixture was adjusted to pH 8 by adding aqueous sodium hydroxide, extracted with ether, washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (15.87 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897387B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-202dabbbe51648bfb8c0746a630daa2a |
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| Source note | uspto-grants-2011_03 |
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