HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572699Generated: October 25, 2026
Nitrogen → 7-Methoxy-1-naphthaleneethanamine
https://huagongshe.com/reaction/572699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | 2-(7-Methoxynaphthalen-1-yl)acetonitrile | HCID 11264068 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Methoxy-1-naphthaleneethanamine | HCID 11052667 | 98% |
Reaction Steps
56 g 7-methoxy-1-naphthaleneacetonitrile, 120 ml ammonia water, 332 ml 95% ethanol, 20 g Raney-Ni were added into autoclave. H2 was introduced after vacuuming it. The operation was repeated for 3 times. The reaction was stirred for 12 hours while H2 was introduced and the condition of 300 atm and 60° C. was maintained. After completion of the reaction, the reaction was kept overnight at room temperature. On the next day, it was vacuumed and N2 gas was introduced. The autoclave was opened up, and the reaction solution was filtered to remove the catalyst. The filtrate was vacuum evaporated until dry to obtain 56 g light green oil. The content is measured as 96.95% by HPLC, and the yield is 95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029420B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-b5a5db2d1d394bd89e4740104ffa279c |
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| Source note | uspto-grants-2015_05 |
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