Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2-Methylindole | HCID 7224 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(Chloromethyl)pyridinium chloride | HCID 74570 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20515681 | HCID 20515681 | — |
Reaction Steps
Methyl iodide (32.0 g) in dry ether (100 ml) was added dropwise to a stirred mixture of magnesium and dry ether (50 ml) at such a rate that the reaction was not too vigorous. After completion of the addition the mixture was heated under reflux for 30 minutes and then cooled to 0°. A solution of 2-methylindole (16.9 g) in dry ether (100 ml) was added dropwise with stirring and the resulting mixture was then heated under reflux for 1.5 hours. It was then cooled to 0° and 4-chloromethyl pyridine hydrochloride (10.5 g) was added portionwise with stirring. The mixture was heated under reflux with stirring for 3 hours and then cooled. A solution of ammonium chloride (30 g) in water (200 ml) was added dropwise with stirring and then the layers were separated. The ether layer was dried (Na2SO4) and evaporated to give an oil which was chromatographed on silica gel. Elution with chloroform initially gave some impurity together with the starting indole. Further elution gave 2-methyl-3-(4-pyridylmethyl)indole (8.0 g), m.p. 126°-127° C. (from ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04363912 |
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| Source dataset | uspto-grants-1982_12 |
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| ORD ID | ord-162644b01e46495d89f6a5ab4be622dc |
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| Source note | uspto-grants-1982_12 |
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