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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375583Generated: October 29, 2026

Potassium Cyanide → 2-Amino-2-cyano-8-chloro-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/375583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantAmmonium ChlorideHCID 25517—
Reactant8-Chloro-1,2,3,4-tetrahydronaphthalen-2-oneHCID 4623269—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Amino-2-cyano-8-chloro-1,2,3,4-tetrahydronaphthaleneHCID 11820321—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a vigorously stirred solution, maintained under nitrogen, containing 277 mmol of 8-chloro-3,4-dihydro-2(1H)-naphthalenone in 350 ml of methanol and 170 ml of water are successively added 282 mmol of potassium cyanide and 290 mmol of ammonium chloride. After stirring for 48 hours at 20° C., the mixture is concentrated. The residue is taken up in ethyl acetate. This organic phase is washed with water and extracted with 1N hydrochloric acid. The acidic phases are basified with 35% sodium hydroxide and extracted with ethyl acetate. The expected product is obtained, in solid form, after drying and evaporating the organic phases.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05486532
Source datasetuspto-grants-1996_01
ORD IDord-cd01ce221b9f41a49778619f4d3f5ee8
Source noteuspto-grants-1996_01