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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233071Generated: October 30, 2026

Water → 3-Amino-4-[methyl-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)amino]benzonitrile

https://huagongshe.com/reaction/2233071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant4-[Methyl-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)amino]-3-nitrobenzonitrileHCID 68464938—
SolventEthyl AcetateHCID 8857—
Product3-Amino-4-[methyl-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)amino]benzonitrileHCID 68467090—

Reaction Conditions

Temperature80 °C

Reaction Steps

SnCl2-2H2O (0.17 mol) is added to a solution of 4-[methyl-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)amino]-3-nitrobenzonitrile (31) (R4=CH3, 34.0 mmol) in EtOAc (125 mL) and the mixture is heated at 80° C. for 1 h. After cooling, to the reaction mixture are successively added 6N NaOH (120 mL), H2O (150 mL), and EtOAc (150 mL). The reaction mixture is filtered through Celite (25 g) and washed with EtOAc. The organic layer is dried over MgSO4 and evaporated in vacuo. The resulting solid is washed with hexane to give (32) (R4=CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709470B2
Source datasetuspto-grants-2010_05
ORD IDord-5216943c3a334fff8314a05d3cbcf181
Source noteuspto-grants-2010_05