HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759443Generated: October 27, 2026
Methanol → alpha-(2-Benzothiazolylthio)-alpha-(m-phenoxyphenyl)propionitrile
https://huagongshe.com/reaction/1759443
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | alpha-(2-Benzothiazolylthio)(m-phenoxyphenyl)acetonitrile | HCID 20532030 | — |
| Solvent | Water | HCID 962 | — |
| Product | alpha-(2-Benzothiazolylthio)-alpha-(m-phenoxyphenyl)propionitrile | HCID 54026807 | 77% |
Reaction Steps
Methanol (5 ml) was added to 945 mg of alpha-(2-benzothiazolylthio)(m-phenoxyphenyl)acetonitrile, and the mixture was stirred under ice cooling in an argon atmosphere. Then, 1.0 ml of a 2.7 M methanol solution of sodium methoxide was added, and the mixture was stirred under ice cooling for 10 minutes. Methyl iodide (0.25 ml) was then added. The mixture was stirred under ice cooling for 30 minutes, and then at room temperature for 2.5 hours. Then, 30 ml of water was added, and the reaction mixture was extracted with 20 ml of methylene chloride three times. The extract was washed with 10 ml of water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel; benzene and methylene chloride) to afford 752 mg (yield 77%) of alpha-(2-benzothiazolylthio)-alpha-(m-phenoxyphenyl)propionitrile as an 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-866a5ed2e4384f828861e7bd29f4e2f9 |
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| Source note | uspto-grants-1982_07 |
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