HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 2-(2-Hydroxy-3-diethylaminomethyl-5-methylphenyl)-2H-benzotriazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Drometrizole | HCID 17113 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 2-(2-Hydroxy-3-diethylaminomethyl-5-methylphenyl)-2H-benzotriazole | HCID 15919022 | — |
Reaction Steps
2-(2-Hydroxy-5-methylphenyl)-2H-benzotriazole (74.3 g, 0.33 mol), diethylamine (37.0 g, 0.51 mol) and paraformaldehyde (17.1 g) are dissolved in 85 mL of n-butanol. The mixture is heated with agitation at reflux (95° to 100° C.) for 44 hours. The solvent is removed by vacuum distillation, and the product, a yellow viscous liquid, is obtained in high yield (>99%). This Mannich base is identified by thin layer chromatography using toluene as the mobile phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05312852 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-5b7849a90615493f9cc28478986725b1 |
| Source note | uspto-grants-1994_05 |