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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52630Generated: October 29, 2026

Potassium Hydroxide → 2-Amino-5-(naphth-2-ylthio)benzonitrile

https://huagongshe.com/reaction/52630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-Nitro-5-(naphth-2-ylthio)benzonitrileHCID 54213165—
SolventHydrochloric AcidHCID 313—
SolventDiglymeHCID 8150—
Product2-Amino-5-(naphth-2-ylthio)benzonitrileHCID 825277103.4%

Reaction Steps

A stirred solution of 13.0 grams (0.042 mole) of 2-nitro-5-(naphth-2-ylthio)benzonitrile in 200 mL of 2-methoxyethyl ether was cooled to 0° C., and a solution of 30.3 grams (0.134 mole) of stannous chloride dihydrate in 91 mL of concentrated hydrochloric acid was added. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature, where it was stirred during a 2 hour period. After this time, the reaction mixture was poured, with stirring, into a mixture of 260 grams of aqueous 50% potassium hydroxide in 300 grams of ice. An oily material, which dropped out of the solution, ultimately solidified. The solid was collected by filtration and was washed with water. The solid was dissolved in methylene chloride and was dried with magnesium sulfate. The mixture was filtered, and the filtrate was concentrated under reduced pressure, yielding 12.0 grams of 2-amino-5-(naphth-2-ylthio)benzonitrile. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616718
Source datasetuspto-grants-1997_04
ORD IDord-e3757a0dafb44c87aebca01d090876dc
Source noteuspto-grants-1997_04