Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | HCID 23681993 | HCID 23681993 | — |
| Product | HCID 10979471 | HCID 10979471 | 84% |
Reaction Steps
Two liter of acetonitrile was added to 510 g of sodium 3-decyloxy-2-naphthalenehydroxamate obtained above, and stirred for about 30 minutes at 60° C. Thereupon, evolution of carbon dioxide gas was confirmed. The reaction mixture was further stirred with heating for 1 hour. Then, the insoluble matter (3,3'-didecyloxy-2-2'-dinaphthylurea) was filtered out, and the filtrate was concentrated. The residue was dissolved in 1 liter of ethyl acetate, and washed 3 times with 500 ml of water. The organic layer was separated from the aqueous layer, dried with Glauber's salt, and then concentrated. Thus, 323 g of whitish orange 3-decyloxy-2-naphthylamine (Compound 1) was obtained in a 84% yield. The melting point of the product was 64°-65.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05354891 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-d1db13db96dd437e91899c508542eb60 |
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| Source note | uspto-grants-1994_10 |
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