Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 3149434 | HCID 3149434 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86662489 | HCID 86662489 | 100.2% |
Reaction Steps
As shown in Chemical Formula 2, an ethanol solution in which 5.03 g (22.0 mmol) of 2-(glycidyloxy)-1-naphthoaldehyde (3) was thoroughly dissolved in 110 mL of ethanol was prepared. Separately, an aqueous solution in which 4.48 g (32.9 mmol) of sodium acetate trihydrate and 2.29 g (32.9 mmol) of hydroxylamine hydrochloride were dissolved in 110 mL of water was prepared. The aqueous solution was added to the ethanol solution and the resultant reaction mixture was stirred at room temperature for 4 hours to effect the reaction. Then, water was added to the reaction mixture and the resultant precipitate was recovered by filtration and was vacuum-dried to obtain 5.36 g (yield: 100%) of 2-(glycidyloxy)-1-naphthoaldehyde oxime (4) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507611B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-b9c25973a388437f9f190d75dd572574 |
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| Source note | uspto-grants-2013_08 |
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