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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (E)-(6-methoxyindan-1-ylidene)acetonitrile | HCID 11830118 | — |
| Reactant | Ammonia methanol | HCID 21705897 | — |
| Catalyst | Cobalt | HCID 104730 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (E)-1-(2-Aminoethylidene)-6-methoxyindan | HCID 10987044 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922771 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-f082034c6aad4a69bf1d1e2e999859cd |
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| Source note | uspto-grants-1999_07 |
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