HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759421Generated: October 25, 2026
Methyl iodide → alpha-(p-Tolylthio)-alpha-(m-phenoxyphenyl)propionitrile
https://huagongshe.com/reaction/1759421
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | alpha-(p-Tolylthio)(m-phenoxyphenyl)-acetonitrile | HCID 12945139 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | alpha-(p-Tolylthio)-alpha-(m-phenoxyphenyl)propionitrile | HCID 13023169 | 86% |
Reaction Steps
1.245 g of alpha-(p-tolylthio)(m-phenoxyphenyl)-acetonitrile was dissolved in 5 ml of anhydrous methanol, and a 2.2 M methanol solution of sodium methoxide was added at room temperature in an atmosphere of argon. The mixture was stirred, and 0.35 ml of methyl iodide was added dropwise. The mixture was further stirred for 30 minutes at room temperature. Then, an aqueous solution of ammonium chloride (3 g/20 ml) was added, and the mixture was extracted with 20 ml of ether three times. The extract was washed with 30 ml of water three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The oily residue was purified by column chromatography (silica gel; hexane and methylene chloride) to afford 1.125 g (yield 86%) of alpha-(p-tolylthio)-alpha-(m-phenoxyphenyl)propionitrile as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04340740 |
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| Source dataset | uspto-grants-1982_07 |
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| ORD ID | ord-41e3db438f8244859a3e784bcced1f33 |
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| Source note | uspto-grants-1982_07 |
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