Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | 2-(5-chloro-2H-benzotriazole-2-yl)-4-(2-hydroxyethyl)phenol | HCID 54477947 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 53790982 | HCID 53790982 | 93.9% |
Reaction Steps
In 25 ml of n-butanol were dissolved 29.0 g (0.1 mols) of the purified product of 2-(5-chloro-2H-benzotriazole-2-yl)-4-(2-hydroxyethyl)phenol synthesized in Example 7, 5.2 g of 80% paraformaldehyde and 11.0 g (0.15 mols) of diethylamine. The solution was refluxed with heating at 105° C. for 24 hours. After completion of the reaction, the solvent and remaining raw materials were collected under reduced pressure, giving 37.0 g of objective 2-(5-chloro-2H-benzotriazole-2-yl)-4-(2-hydroxyethyl)-6-(N,N-diethylaminomethyl)phenol as a brown oil (yield 93.9%, purity 95.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922882 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-14805592f3034e5d9fa36f108851f51c |
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| Source note | uspto-grants-1999_07 |
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