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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582201Generated: October 29, 2026

(E)-(6-methoxyindan-1-ylidene)acetonitrile → (E)-1-(2-Aminoethylidene)-6-methoxyindan

https://huagongshe.com/reaction/582201

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-(6-methoxyindan-1-ylidene)acetonitrileHCID 11830118—
ReactantAmmonia methanolHCID 21705897—
CatalystCobaltHCID 104730—
SolventEthanolHCID 702—
Product(E)-1-(2-Aminoethylidene)-6-methoxyindanHCID 1098704486%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of (E)-(6-methoxyindan-1-ylidene)acetonitrile (1.60 g, 8.64 mmol.) in ethanol (80 ml) were added a 2M ammonia/methanol solution (40 ml) and Raney cobalt (1.6 g). The reaction mixture was stirred, under hydrogen atmosphere (4 kgf/cm2) for 32 hours at 40° C. and for further 8 hours at 70° C. The Raney cobalt was filtered off, and then the solvent was distilled off. The residue was purified by means of a silica gel column chromatography (chloroform:methanol=9:1 to chloroform:methanol:triethylamine=90:8:2) to afford the titled compound (1.40 g, yield 86%, oily).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922771
Source datasetuspto-grants-1999_07
ORD IDord-f082034c6aad4a69bf1d1e2e999859cd
Source noteuspto-grants-1999_07