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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128713Generated: October 24, 2026

Potassium Cyanide → 2-Amino-2-cyano-5-methoxy-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/en/reaction/128713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Methoxy-2-tetraloneHCID 259194—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-Amino-2-cyano-5-methoxy-1,2,3,4-tetrahydronaphthaleneHCID 9990431—

Reaction Steps

112 mmol of potassium cyanide and 116 mmol of ammonium chloride ate added successively to a solution, maintained under nitrogen and with stirring, containing 110 mmol of 5-methoxy-3,4-dihydronaphthalen-2(1H)-one in 90 ml of ethanol and 50 ml of water. The whole mixture is stirred for 20 hours at 20° C. and then concentrated under vacuum. The residue is taken up in 200 ml of ethyl acetate. This phase is then washed with water and extracted with 1N hydrochloric acid. The acid phase is basified with 35% sodium hydroxide solution and extracted with methyl acetate. The combined organic phases are dried and evaporated under vacuum and lead to the expected product in the solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464859
Source datasetuspto-grants-1995_11
ORD IDord-ba8afc10f72a433885205de1993275b0
Source noteuspto-grants-1995_11