Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Benzene, 1-(chloromethyl)-2-fluoro- | HCID 9580 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Methyl-2,3-dihydroisoquinolin-4(1H)-one | HCID 10630812 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15917418 | HCID 15917418 | — |
Reaction Steps
To a suspension of magnesium shavings (3.96 g) and a crystal of iodine in anhydrous ether (50 ml) is added several milliliters of 2-fluorobenzyl chloride. After initiation of the reaction with a hot air gun, the remainder of the 2-fluorobenzyl chloride for a total of 27.2 g is added dropwise as a solution in ether (50 ml). After the addition is complete, the reaction mixture is refluxed for 2 hours. A solution of 2-methyl-2,3-dihydro-4(1H)-isoquinolone (24.2 g) in ether (100 ml) is added dropwise at room temperature. The granular precipitate which forms is stirred at room temperature for one hour, filtered and washed with ether. The solid is hydrolyzed by stirring at room temperature for one hour with an ammonium chloride solution, followed by ether extraction. The ether extract is washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. Removal of the ether yields 28.6 g of an oil. A portion of the oil (5 g) is dissolved in ether, filtered, and ethereal hydrogen chloride is added to give product as a white powder (5.5 g, 97%), mp 105°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04410699 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-0cc5c266da3b41e1a7e3d4b837f0180e |
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| Source note | uspto-grants-1983_10 |
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