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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl iodideHCID 6328—
ReactantSodium MethoxideHCID 10942334—
Reactantalpha-(2-Benzothiazolylthio)(m-phenoxyphenyl)acetonitrileHCID 20532030—
SolventWaterHCID 962—
Productalpha-(2-Benzothiazolylthio)-alpha-(m-phenoxyphenyl)propionitrileHCID 5402680777%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04340740
Source datasetuspto-grants-1982_07
ORD IDord-866a5ed2e4384f828861e7bd29f4e2f9
Source noteuspto-grants-1982_07