Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hexadecylamine | HCID 8926 | — |
| Reactant | HCID 12067418 | HCID 12067418 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12067413 | HCID 12067413 | 35.9% |
Reaction Steps
A dispersion of 6.5 g of 2-hydroxy-3-phenylaminocarbonyl-6-chlorocarbonylnaphthalene in 20.0 g of dry tetrahydrofuran was added with 9.2 g of n-hexadecylamine solution in 30 g of dry tetrahydrofuran and reacted under reflux for 12 hours. To the reaction mixture, 30 g of water was added and the precipitates were collected by filtration, washed with water and thus obtained crystal was washed with 30 g of methanol under reflux. The obtained mixture was cooled to 30° C. and filtrated, washed with methanol and dried to provide 3.8 g of 2-hydroxy-3-phenylaminocarbonyl-6-n-hexadecylaminocarbonyl naphthalene (decomposition point: 257.2° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548703B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-9f74a8a152fb4ce390e9a653f827b5d8 |
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| Source note | uspto-grants-2003_04 |
|---|